|
ENST00000367698.4:c.1301T=
MANE Select
|
ENSP00000356671.3:p.Phe434=
|
|
|
ENST00000367698.3:c.1301T=
|
ENSP00000356671.3:p.Phe434=
|
|
|
ENST00000617423.4:c.686T=
|
ENSP00000478688.1:p.Phe229=
|
|
|
NM_000488.3:c.1301T= , LRG_577t1:c.1301T=
|
NP_000479.1:p.Phe434=
|
|
|
XM_005245198.2:c.1157T=
|
XP_005245255.1:p.Phe386=
|
|
|
NM_001365052.1:c.1157T=
|
NP_001351981.1:p.Phe386=
|
|
|
NM_000488.4:c.1301T=
MANE Select
|
NP_000479.1:p.Phe434=
|
|
|
NM_001365052.2:c.1157T=
|
NP_001351981.1:p.Phe386=
|
|
|
NM_001386302.1:c.1424T=
|
NP_001373231.1:p.Phe475=
|
|
|
NM_001386303.1:c.1382T=
|
NP_001373232.1:p.Phe461=
|
|
|
NM_001386304.1:c.1280T=
|
NP_001373233.1:p.Phe427=
|
|
|
NM_001386305.1:c.1244T=
|
NP_001373234.1:p.Phe415=
|
|
|
NM_001386306.1:c.1085T=
|
NP_001373235.1:p.Phe362=
|
|
