NM_004525.3:c.13919A>T
MANE Select
|
NP_004516.2:p.Asp4640Val
|
ENST00000649046.1:c.13919A>T
MANE Select
|
ENSP00000496870.1:p.Asp4640Val
|
NM_004525.2:c.13919A>T
|
NP_004516.2:p.Asp4640Val
|
ENST00000263816.7:c.13919A>T
|
ENSP00000263816.3:p.Asp4640Val
|
ENST00000649153.1:c.4728A>T
|
|
ENST00000650252.1:c.2910A>T
|
ENSP00000496887.1:n.2910A>T
|
XM_011511183.1:c.13790A>T
|
XP_011509485.1:p.Asp4597Val
|
XM_011511183.3:c.13790A>T
|
XP_011509485.1:p.Asp4597Val
|
XM_011511184.1:c.11630A>T
|
XP_011509486.1:p.Asp3877Val
|
XM_011511184.2:c.11630A>T
|
XP_011509486.1:p.Asp3877Val
|