ENST00000617875.6:c.3394-58C>A
MANE Select
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ENSP00000482313.2:n.3394-58C>A
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ENST00000301323.7:c.411-58C>A
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|
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ENST00000529424.2:n.50-58C>A
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|
|
ENST00000531875.2:c.648+55C>A
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ENSP00000477910.1:n.648+55C>A
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|
ENST00000617875.4:c.3394-58C>A
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ENSP00000482313.1:n.3394-58C>A
|
|
ENST00000621189.4:c.2323-58C>A
|
ENSP00000483145.1:n.2323-58C>A
|
|
NM_004260.3:c.3394-58C>A
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NP_004251.3:n.3394-58C>A
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|
XM_011517380.1:c.3469-58C>A
|
XP_011515682.1:n.3469-58C>A
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|
XM_011517381.1:c.3373-58C>A
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XP_011515683.1:n.3373-58C>A
|
|
XM_011517382.1:c.3277-58C>A
|
XP_011515684.1:n.3277-58C>A
|
|
XM_011517383.1:c.3271-58C>A
|
XP_011515685.1:n.3271-58C>A
|
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XM_011517384.1:c.3196-58C>A
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XP_011515686.1:n.3196-58C>A
|
|
XM_011517385.1:c.2332-58C>A
|
XP_011515687.1:n.2332-58C>A
|
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XR_928366.1:n.3353-58C>A
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|
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XR_928367.1:n.3449-58C>A
|
|
|
XR_928368.1:n.3342-58C>A
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|
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XM_011517384.3:c.3196-58C>A
|
XP_011515686.1:n.3196-58C>A
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|
XM_017013991.2:c.3622C>A
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XP_016869480.1:p.Leu1208Ile
|
|
XM_017013992.2:c.3547C>A
|
XP_016869481.1:p.Leu1183Ile
|
|
XM_017013993.2:c.3532C>A
|
XP_016869482.1:p.Leu1178Ile
|
|
XM_017013994.2:c.3526C>A
|
XP_016869483.1:p.Leu1176Ile
|
|
XM_017013995.2:c.3457C>A
|
XP_016869484.1:p.Leu1153Ile
|
|
XM_017013996.2:c.3559-58C>A
|
XP_016869485.1:n.3559-58C>A
|
|
XM_017013997.2:c.3424C>A
|
XP_016869486.1:p.Leu1142Ile
|
|
XM_017013998.1:c.3484-58C>A
|
XP_016869487.1:n.3484-58C>A
|
|
XM_017013999.2:c.3334C>A
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XP_016869488.1:p.Leu1112Ile
|
|
XM_017014000.1:c.2485C>A
|
XP_016869489.1:p.Leu829Ile
|
|
XM_017014001.2:c.2395C>A
|
XP_016869490.1:p.Leu799Ile
|
|
XR_001745626.2:n.3439-58C>A
|
|
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XR_001745627.2:n.3535-58C>A
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XR_001745628.2:n.3426-58C>A
|
|
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XR_001745629.2:n.3289-58C>A
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|
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XR_001745630.2:n.3091-58C>A
|
|
|
NM_004260.4:c.3394-58C>A
MANE Select
|
NP_004251.4:n.3394-58C>A
|
|