ENST00000343307.5:c.1184G>T
MANE Select
|
ENSP00000343002.4:p.Gly395Val
|
|
ENST00000343307.4:c.1184G>T
|
ENSP00000343002.4:p.Gly395Val
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|
NM_194318.3:c.1184G>T
|
NP_919299.3:p.Gly395Val
|
|
XM_006719768.2:c.1127G>T
|
XP_006719831.1:p.Gly376Val
|
|
XM_011534936.1:c.1065-6066G>T
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XP_011533238.1:n.1065-6066G>T
|
|
XM_011534937.1:c.1064G>T
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XP_011533239.1:p.Gly355Val
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|
XM_011534938.1:c.1037G>T
|
XP_011533240.1:p.Gly346Val
|
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XM_006719768.3:c.1127G>T
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XP_006719831.1:p.Gly376Val
|
|
XM_011534938.2:c.1037G>T
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XP_011533240.1:p.Gly346Val
|
|
XM_017020395.1:c.1037G>T
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XP_016875884.1:p.Gly346Val
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|
NM_194318.4:c.1184G>T
MANE Select
|
NP_919299.3:p.Gly395Val
|
|