|
ENST00000367698.4:c.1248A=
MANE Select
|
ENSP00000356671.3:p.Ala416=
|
|
|
ENST00000367698.3:c.1248A=
|
ENSP00000356671.3:p.Ala416=
|
|
|
ENST00000617423.4:c.633A=
|
ENSP00000478688.1:p.Ala211=
|
|
|
NM_000488.3:c.1248A= , LRG_577t1:c.1248A=
|
NP_000479.1:p.Ala416=
|
|
|
XM_005245198.2:c.1104A=
|
XP_005245255.1:p.Ala368=
|
|
|
NM_001365052.1:c.1104A=
|
NP_001351981.1:p.Ala368=
|
|
|
NM_000488.4:c.1248A=
MANE Select
|
NP_000479.1:p.Ala416=
|
|
|
NM_001365052.2:c.1104A=
|
NP_001351981.1:p.Ala368=
|
|
|
NM_001386302.1:c.1371A=
|
NP_001373231.1:p.Ala457=
|
|
|
NM_001386303.1:c.1329A=
|
NP_001373232.1:p.Ala443=
|
|
|
NM_001386304.1:c.1227A=
|
NP_001373233.1:p.Ala409=
|
|
|
NM_001386305.1:c.1191A=
|
NP_001373234.1:p.Ala397=
|
|
|
NM_001386306.1:c.1032A=
|
NP_001373235.1:p.Ala344=
|
|
