ENST00000450053.8:c.3808G>T
MANE Select
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ENSP00000415034.2:p.Gly1270Ter
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ENST00000651747.1:c.3706G>T
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ENSP00000499216.1:p.Gly1236Ter
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ENST00000652744.1:n.145G>T
|
|
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ENST00000416683.5:c.1960-289G>T
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ENST00000450053.7:c.3808G>T
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ENSP00000415034.2:p.Gly1270Ter
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NM_015175.2:c.3808G>T , LRG_568t1:c.3808G>T
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NP_055990.1:p.Gly1270Ter
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XM_005264992.2:c.3706G>T
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XP_005265049.1:p.Gly1236Ter
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XM_005264993.2:c.280G>T
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XP_005265050.1:p.Gly94Ter
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XM_006713072.2:c.3727G>T
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XP_006713135.1:p.Gly1243Ter
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XM_011533532.1:c.3787G>T
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XP_011531834.1:p.Gly1263Ter
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XM_011533533.1:c.3808G>T
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XP_011531835.1:p.Gly1270Ter
|
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XM_011533534.1:c.3439G>T
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XP_011531836.1:p.Gly1147Ter
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XM_011533535.1:c.3268G>T
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XP_011531837.1:p.Gly1090Ter
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XM_011533536.1:c.3154G>T
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XP_011531838.1:p.Gly1052Ter
|
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XM_011533537.1:c.2716G>T
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XP_011531839.1:p.Gly906Ter
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XR_940397.1:n.3984G>T
|
|
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XR_940398.1:n.3984G>T
|
|
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NM_001365116.1:c.3706G>T
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NP_001352045.1:p.Gly1236Ter
|
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XM_006713072.3:c.3727G>T
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XP_006713135.1:p.Gly1243Ter
|
|
XM_011533533.2:c.3808G>T
|
XP_011531835.1:p.Gly1270Ter
|
|
XM_017006010.1:c.3808G>T
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XP_016861499.1:p.Gly1270Ter
|
|
XM_017006011.1:c.3787G>T
|
XP_016861500.1:p.Gly1263Ter
|
|
XM_017006012.1:c.3727G>T
|
XP_016861501.1:p.Gly1243Ter
|
|
XM_017006013.1:c.3808G>T
|
XP_016861502.1:p.Gly1270Ter
|
|
XM_017006014.1:c.3706G>T
|
XP_016861503.1:p.Gly1236Ter
|
|
XM_017006015.1:c.3439G>T
|
XP_016861504.1:p.Gly1147Ter
|
|
XM_017006016.1:c.3268G>T
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XP_016861505.1:p.Gly1090Ter
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|
XM_017006017.1:c.280G>T
|
XP_016861506.1:p.Gly94Ter
|
|
XR_940397.2:n.3984G>T
|
|
|
NM_001365116.2:c.3706G>T
|
NP_001352045.1:p.Gly1236Ter
|
|
NM_015175.3:c.3808G>T
MANE Select
|
NP_055990.1:p.Gly1270Ter
|
|