ENST00000343307.5:c.1181G>T
MANE Select
|
ENSP00000343002.4:p.Gly394Val
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|
ENST00000343307.4:c.1181G>T
|
ENSP00000343002.4:p.Gly394Val
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|
NM_194318.3:c.1181G>T
|
NP_919299.3:p.Gly394Val
|
|
XM_006719768.2:c.1124G>T
|
XP_006719831.1:p.Gly375Val
|
|
XM_011534936.1:c.1065-6069G>T
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XP_011533238.1:n.1065-6069G>T
|
|
XM_011534937.1:c.1061G>T
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XP_011533239.1:p.Gly354Val
|
|
XM_011534938.1:c.1034G>T
|
XP_011533240.1:p.Gly345Val
|
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XM_006719768.3:c.1124G>T
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XP_006719831.1:p.Gly375Val
|
|
XM_011534938.2:c.1034G>T
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XP_011533240.1:p.Gly345Val
|
|
XM_017020395.1:c.1034G>T
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XP_016875884.1:p.Gly345Val
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|
NM_194318.4:c.1181G>T
MANE Select
|
NP_919299.3:p.Gly394Val
|
|