ENST00000367698.4:c.1335A>T
MANE Select
|
ENSP00000356671.3:p.Arg445Ser
|
|
ENST00000367698.3:c.1335A>T
|
ENSP00000356671.3:p.Arg445Ser
|
|
ENST00000617423.4:c.720A>T
|
ENSP00000478688.1:p.Arg240Ser
|
|
NM_000488.3:c.1335A>T , LRG_577t1:c.1335A>T
|
NP_000479.1:p.Arg445Ser
|
|
XM_005245198.2:c.1191A>T
|
XP_005245255.1:p.Arg397Ser
|
|
NM_001365052.1:c.1191A>T
|
NP_001351981.1:p.Arg397Ser
|
|
NM_000488.4:c.1335A>T
MANE Select
|
NP_000479.1:p.Arg445Ser
|
|
NM_001365052.2:c.1191A>T
|
NP_001351981.1:p.Arg397Ser
|
|
NM_001386302.1:c.1458A>T
|
NP_001373231.1:p.Arg486Ser
|
|
NM_001386303.1:c.1416A>T
|
NP_001373232.1:p.Arg472Ser
|
|
NM_001386304.1:c.1314A>T
|
NP_001373233.1:p.Arg438Ser
|
|
NM_001386305.1:c.1278A>T
|
NP_001373234.1:p.Arg426Ser
|
|
NM_001386306.1:c.1119A>T
|
NP_001373235.1:p.Arg373Ser
|
|