ENST00000299314.12:c.3491T>G
MANE Select
|
ENSP00000299314.7:p.Val1164Gly
|
|
ENST00000299314.11:c.3491T>G
|
ENSP00000299314.7:p.Val1164Gly
|
|
ENST00000549738.5:c.389T>G
|
ENSP00000450161.1:n.389T>G
|
|
NM_024312.4:c.3491T>G
|
NP_077288.2:p.Val1164Gly
|
|
XM_011538731.1:c.3410T>G
|
XP_011537033.1:p.Val1137Gly
|
|
XM_011538731.2:c.3410T>G
|
XP_011537033.1:p.Val1137Gly
|
|
XM_017019961.1:c.3275T>G
|
XP_016875450.1:p.Val1092Gly
|
|
XM_017019962.2:c.2264T>G
|
XP_016875451.1:p.Val755Gly
|
|
NM_024312.5:c.3491T>G
MANE Select
|
NP_077288.2:p.Val1164Gly
|
|