ENST00000649046.1:c.12260T>G
MANE Select
|
ENSP00000496870.1:p.Val4087Gly
|
|
ENST00000649153.1:c.3160T>G
|
|
|
ENST00000650252.1:c.1288T>G
|
ENSP00000496887.1:p.Leu430Val
|
|
ENST00000263816.7:c.12260T>G
|
ENSP00000263816.3:p.Val4087Gly
|
|
NM_004525.2:c.12260T>G
|
NP_004516.2:p.Val4087Gly
|
|
XM_011511183.1:c.12131T>G
|
XP_011509485.1:p.Val4044Gly
|
|
XM_011511184.1:c.9971T>G
|
XP_011509486.1:p.Val3324Gly
|
|
NM_004525.3:c.12260T>G
MANE Select
|
NP_004516.2:p.Val4087Gly
|
|
XM_011511183.3:c.12131T>G
|
XP_011509485.1:p.Val4044Gly
|
|
XM_011511184.2:c.9971T>G
|
XP_011509486.1:p.Val3324Gly
|
|