ENST00000681320.1:c.7415G>C
MANE Select
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ENSP00000506558.1:p.Gly2472Ala
|
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ENST00000328333.12:c.7415G>C
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ENSP00000332371.8:p.Gly2472Ala
|
|
ENST00000422991.1:c.410G>C
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ENSP00000391608.1:p.Gly137Ala
|
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ENST00000459756.5:n.142G>C
|
|
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ENST00000467985.1:n.165G>C
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|
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ENST00000487017.5:n.4054G>C
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|
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NM_000094.3:c.7415G>C , LRG_286t1:c.7415G>C
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NP_000085.1:p.Gly2472Ala
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|
XM_011533336.1:c.7442G>C
|
XP_011531638.1:p.Gly2481Ala
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XM_011533337.1:c.7415G>C
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XP_011531639.1:p.Gly2472Ala
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XM_011533338.1:c.7408-122G>C
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XP_011531640.1:n.7408-122G>C
|
|
XM_011533339.1:c.7442G>C
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XP_011531641.1:p.Gly2481Ala
|
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XM_011533340.1:c.7408-48G>C
|
XP_011531642.1:n.7408-48G>C
|
|
XM_011533341.1:c.7382-48G>C
|
XP_011531643.1:n.7382-48G>C
|
|
XM_011533342.1:c.7382-122G>C
|
XP_011531644.1:n.7382-122G>C
|
|
XR_940369.1:n.7478G>C
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|
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XR_940370.1:n.7478G>C
|
|
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XR_940371.1:n.7478G>C
|
|
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XR_940372.1:n.7452G>C
|
|
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XM_017005688.1:c.7381-122G>C
|
XP_016861177.1:n.7381-122G>C
|
|
XM_017005689.1:c.7415G>C
|
XP_016861178.1:p.Gly2472Ala
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XM_017005690.1:c.7381-48G>C
|
XP_016861179.1:n.7381-48G>C
|
|
XM_017005691.1:c.7355-48G>C
|
XP_016861180.1:n.7355-48G>C
|
|
XM_017005692.1:c.7355-122G>C
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XP_016861181.1:n.7355-122G>C
|
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XR_001740003.1:n.7451G>C
|
|
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XR_001740004.1:n.7451G>C
|
|
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XR_001740005.1:n.7451G>C
|
|
|
XR_001740006.1:n.7425G>C
|
|
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NM_000094.4:c.7415G>C
MANE Select
|
NP_000085.1:p.Gly2472Ala
|
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