ENST00000299314.12:c.3588T>G
MANE Select
|
ENSP00000299314.7:p.His1196Gln
|
|
ENST00000299314.11:c.3588T>G
|
ENSP00000299314.7:p.His1196Gln
|
|
ENST00000549738.5:c.486T>G
|
ENSP00000450161.1:n.486T>G
|
|
NM_024312.4:c.3588T>G
|
NP_077288.2:p.His1196Gln
|
|
XM_011538731.1:c.3507T>G
|
XP_011537033.1:p.His1169Gln
|
|
XM_011538731.2:c.3507T>G
|
XP_011537033.1:p.His1169Gln
|
|
XM_017019961.1:c.3372T>G
|
XP_016875450.1:p.His1124Gln
|
|
XM_017019962.2:c.2361T>G
|
XP_016875451.1:p.His787Gln
|
|
NM_024312.5:c.3588T>G
MANE Select
|
NP_077288.2:p.His1196Gln
|
|