ENST00000367698.4:c.1291A>T
MANE Select
|
ENSP00000356671.3:p.Arg431Trp
|
|
ENST00000367698.3:c.1291A>T
|
ENSP00000356671.3:p.Arg431Trp
|
|
ENST00000617423.4:c.676A>T
|
ENSP00000478688.1:p.Arg226Trp
|
|
NM_000488.3:c.1291A>T , LRG_577t1:c.1291A>T
|
NP_000479.1:p.Arg431Trp
|
|
XM_005245198.2:c.1147A>T
|
XP_005245255.1:p.Arg383Trp
|
|
NM_001365052.1:c.1147A>T
|
NP_001351981.1:p.Arg383Trp
|
|
NM_000488.4:c.1291A>T
MANE Select
|
NP_000479.1:p.Arg431Trp
|
|
NM_001365052.2:c.1147A>T
|
NP_001351981.1:p.Arg383Trp
|
|
NM_001386302.1:c.1414A>T
|
NP_001373231.1:p.Arg472Trp
|
|
NM_001386303.1:c.1372A>T
|
NP_001373232.1:p.Arg458Trp
|
|
NM_001386304.1:c.1270A>T
|
NP_001373233.1:p.Arg424Trp
|
|
NM_001386305.1:c.1234A>T
|
NP_001373234.1:p.Arg412Trp
|
|
NM_001386306.1:c.1075A>T
|
NP_001373235.1:p.Arg359Trp
|
|