ENST00000330342.8:c.1373G>T
MANE Select
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ENSP00000332247.2:p.Gly458Val
|
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ENST00000540368.6:n.1404G>T
|
|
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ENST00000674794.1:c.1461G>T
|
|
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ENST00000675260.1:n.648G>T
|
|
|
ENST00000675344.1:c.*394G>T
|
ENSP00000501953.1:n.*394G>T
|
|
ENST00000330342.7:c.1373G>T
|
ENSP00000332247.2:p.Gly458Val
|
|
ENST00000504192.2:c.983G>T
|
ENSP00000443441.1:p.Gly328Val
|
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ENST00000536426.1:n.390G>T
|
|
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ENST00000545059.5:n.4009G>T
|
|
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NM_012463.3:c.1373G>T
|
NP_036595.2:p.Gly458Val
|
|
XM_005253563.1:c.1373G>T
|
XP_005253620.1:p.Gly458Val
|
|
XM_006719317.2:c.860G>T
|
XP_006719380.1:p.Gly287Val
|
|
XM_006719318.2:c.551G>T
|
XP_006719381.1:p.Gly184Val
|
|
XR_429088.1:n.1536G>T
|
|
|
XM_024448910.1:c.1373G>T
|
XP_024304678.1:p.Gly458Val
|
|
XM_024448911.1:c.860G>T
|
XP_024304679.1:p.Gly287Val
|
|
XM_024448912.1:c.551G>T
|
XP_024304680.1:p.Gly184Val
|
|
NM_012463.4:c.1373G>T
MANE Select
|
NP_036595.2:p.Gly458Val
|
|