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ENST00000529967.6:n.735-293G>T
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ENST00000642611.2:n.2545-293G>T
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ENST00000682051.1:n.2492-293G>T
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|
ENST00000682110.1:n.2545-293G>T
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ENST00000682140.1:c.2473-293G>T
|
ENSP00000507829.1:n.2473-293G>T
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|
ENSP00000507094.1:n.*614-293G>T
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ENST00000682215.1:n.2542-293G>T
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|
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ENST00000682528.1:n.2542-293G>T
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ENST00000682673.1:n.2489-293G>T
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ENST00000682805.1:n.2542-293G>T
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ENST00000682965.1:c.2473-293G>T
|
ENSP00000508229.1:n.2473-293G>T
|
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ENST00000683093.1:n.2644-293G>T
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|
ENSP00000507768.1:n.2473-293G>T
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ENST00000683153.1:n.2701-293G>T
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ENST00000683365.1:n.2647-293G>T
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ENST00000683377.1:n.2545-293G>T
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ENST00000683456.1:c.2476-293G>T
|
ENSP00000508318.1:n.2476-293G>T
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ENST00000683522.1:n.2545-293G>T
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|
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|
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|
ENSP00000508265.1:n.*645-293G>T
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ENST00000683693.1:n.2542-293G>T
|
|
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|
ENST00000683725.1:c.2476-293G>T
|
ENSP00000507496.1:n.2476-293G>T
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ENST00000684010.1:n.2460-293G>T
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ENST00000684157.1:n.2545-293G>T
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ENST00000684288.1:c.*648-293G>T
|
ENSP00000507143.1:n.*648-293G>T
|
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ENST00000684313.1:n.1977-293G>T
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ENST00000684332.1:n.2618-293G>T
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ENST00000684371.1:n.2651-293G>T
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ENST00000684404.1:n.2542-293G>T
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ENST00000684442.1:n.2545-293G>T
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|
ENST00000684555.1:c.*688-293G>T
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ENSP00000507705.1:n.*688-293G>T
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ENST00000684571.1:c.2317-293G>T
|
ENSP00000506935.1:n.2317-293G>T
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ENST00000684593.1:c.*2181-293G>T
|
ENSP00000507005.1:n.*2181-293G>T
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|
ENSP00000506841.1:n.*872-293G>T
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ENST00000302539.9:c.2479-293G>T
|
ENSP00000303960.4:n.2479-293G>T
|
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|
ENST00000389817.8:c.2476-293G>T
MANE Select
|
ENSP00000374467.4:n.2476-293G>T
|
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ENST00000642271.1:c.2473-293G>T
|
ENSP00000493749.1:n.2473-293G>T
|
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ENST00000642579.1:c.560-293G>T
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ENST00000642611.1:n.2430-293G>T
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|
ENST00000642902.1:c.2311-293G>T
|
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|
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|
ENSP00000494450.1:n.2476-293G>T
|
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|
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|
ENSP00000496124.1:n.*452-293G>T
|
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ENST00000643925.1:c.416-62G>T
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|
ENST00000644447.1:c.832-293G>T
|
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|
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|
ENSP00000495378.1:n.*837-293G>T
|
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|
ENST00000644484.1:c.*685-293G>T
|
ENSP00000493558.1:n.*685-293G>T
|
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|
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|
ENSP00000495532.1:n.*2181-293G>T
|
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|
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|
ENSP00000494567.1:n.*648-293G>T
|
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|
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|
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|
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|
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|
ENSP00000494321.1:n.2542-293G>T
|
|
|
ENST00000645076.1:c.1728-293G>T
|
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|
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|
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|
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|
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|
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|
ENSP00000495516.1:n.2476-293G>T
|
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|
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|
ENSP00000495259.1:n.*532-293G>T
|
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|
ENSP00000495025.1:n.*840-293G>T
|
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|
ENST00000646276.1:c.*749-293G>T
|
ENSP00000496070.1:n.*749-293G>T
|
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ENST00000646592.1:c.1702-293G>T
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|
ENST00000646902.1:c.2473-293G>T
|
ENSP00000494101.1:n.2473-293G>T
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ENST00000646993.1:c.*872-293G>T
|
ENSP00000493720.1:n.*872-293G>T
|
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|
ENSP00000496741.1:n.2482-293G>T
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|
ENST00000647015.1:c.2227-293G>T
|
ENSP00000495389.1:n.2227-293G>T
|
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|
ENST00000647086.1:c.*2206-293G>T
|
ENSP00000493677.1:n.*2206-293G>T
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|
ENST00000647158.1:c.*617-293G>T
|
ENSP00000495744.1:n.*617-293G>T
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ENST00000302539.8:c.2479-293G>T
|
ENSP00000303960.4:n.2479-293G>T
|
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|
ENST00000389817.7:c.2476-293G>T
|
ENSP00000374467.3:n.2476-293G>T
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ENST00000526921.5:n.160-293G>T
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|
ENST00000527905.5:c.2446-293G>T
|
ENSP00000431653.1:n.2446-293G>T
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ENST00000529967.5:n.145-293G>T
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ENST00000530147.5:n.59-293G>T
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|
ENST00000531911.1:n.590-293G>T
|
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|
NM_000352.4:c.2476-293G>T
|
NP_000343.2:n.2476-293G>T
|
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|
NM_001287174.1:c.2479-293G>T
|
NP_001274103.1:n.2479-293G>T
|
|
|
XM_011520331.1:c.2476-293G>T
|
XP_011518633.1:n.2476-293G>T
|
|
|
XM_011520332.1:c.2479-293G>T
|
XP_011518634.1:n.2479-293G>T
|
|
|
XM_011520333.1:c.976-293G>T
|
XP_011518635.1:n.976-293G>T
|
|
|
XM_011520334.1:c.2479-293G>T
|
XP_011518636.1:n.2479-293G>T
|
|
|
XR_930890.1:n.2542-293G>T
|
|
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|
XR_930891.1:n.2542-293G>T
|
|
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|
XR_930892.1:n.2542-293G>T
|
|
|
|
XR_930893.1:n.2539-293G>T
|
|
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|
NM_001351295.1:c.2542-293G>T
|
NP_001338224.1:n.2542-293G>T
|
|
|
NM_001351296.1:c.2476-293G>T
|
NP_001338225.1:n.2476-293G>T
|
|
|
NM_001351297.1:c.2473-293G>T
|
NP_001338226.1:n.2473-293G>T
|
|
|
NR_147094.1:n.2545-293G>T
|
|
|
|
XM_017018197.2:c.2545-293G>T
|
XP_016873686.1:n.2545-293G>T
|
|
|
XM_017018199.1:c.2542-293G>T
|
XP_016873688.1:n.2542-293G>T
|
|
|
XM_017018201.2:c.2545-293G>T
|
XP_016873690.1:n.2545-293G>T
|
|
|
XM_017018202.1:c.1042-293G>T
|
XP_016873691.1:n.1042-293G>T
|
|
|
XM_017018204.1:c.433-293G>T
|
XP_016873693.1:n.433-293G>T
|
|
|
XM_024448668.1:c.844-293G>T
|
XP_024304436.1:n.844-293G>T
|
|
|
XR_001747945.2:n.2617-293G>T
|
|
|
|
XR_001747946.2:n.2548-293G>T
|
|
|
|
XR_002957189.1:n.2617-293G>T
|
|
|
|
NM_000352.6:c.2476-293G>T
MANE Select
|
NP_000343.2:n.2476-293G>T
|
|
|
NM_001287174.2:c.2479-293G>T
|
NP_001274103.1:n.2479-293G>T
|
|
|
NM_001351295.2:c.2542-293G>T
|
NP_001338224.1:n.2542-293G>T
|
|
|
NM_001351296.2:c.2476-293G>T
|
NP_001338225.1:n.2476-293G>T
|
|
|
NM_001351297.2:c.2473-293G>T
|
NP_001338226.1:n.2473-293G>T
|
|
|
NR_147094.2:n.2545-293G>T
|
|
|
|
NM_001287174.3:c.2479-293G>T
|
NP_001274103.1:n.2479-293G>T
|
|
