ENST00000299314.12:c.3564T>G
MANE Select
|
ENSP00000299314.7:p.Tyr1188Ter
|
|
ENST00000299314.11:c.3564T>G
|
ENSP00000299314.7:p.Tyr1188Ter
|
|
ENST00000549738.5:c.462T>G
|
ENSP00000450161.1:n.462T>G
|
|
NM_024312.4:c.3564T>G
|
NP_077288.2:p.Tyr1188Ter
|
|
XM_011538731.1:c.3483T>G
|
XP_011537033.1:p.Tyr1161Ter
|
|
XM_011538731.2:c.3483T>G
|
XP_011537033.1:p.Tyr1161Ter
|
|
XM_017019961.1:c.3348T>G
|
XP_016875450.1:p.Tyr1116Ter
|
|
XM_017019962.2:c.2337T>G
|
XP_016875451.1:p.Tyr779Ter
|
|
NM_024312.5:c.3564T>G
MANE Select
|
NP_077288.2:p.Tyr1188Ter
|
|