ENST00000370192.8:c.1495G>T
MANE Select
|
ENSP00000359211.3:p.Ala499Ser
|
|
ENST00000370192.7:c.1495G>T
|
ENSP00000359211.3:p.Ala499Ser
|
|
NM_000110.3:c.1495G>T , LRG_722t1:c.1495G>T
|
NP_000101.2:p.Ala499Ser
|
|
XM_005270562.3:c.1495G>T
|
XP_005270619.2:p.Ala499Ser
|
|
XM_006710397.2:c.1495G>T
|
XP_006710460.1:p.Ala499Ser
|
|
XM_006710397.3:c.1495G>T
|
XP_006710460.1:p.Ala499Ser
|
|
XM_017000507.1:c.1384G>T
|
XP_016855996.1:p.Ala462Ser
|
|
XM_017000508.2:c.1000G>T
|
XP_016855997.1:p.Ala334Ser
|
|
XM_017000509.2:c.1000G>T
|
XP_016855998.1:p.Ala334Ser
|
|
XM_017000510.1:c.1000G>T
|
XP_016855999.1:p.Ala334Ser
|
|
NM_000110.4:c.1495G>T
MANE Select
|
NP_000101.2:p.Ala499Ser
|
|