ENST00000541682.7:c.342C>T
MANE Select
|
ENSP00000446205.2:p.Asp114=
|
|
ENST00000317814.8:c.327C>T
|
ENSP00000314774.4:p.Asp109=
|
|
ENST00000541682.6:c.342C>T
|
ENSP00000446205.2:p.Asp114=
|
|
ENST00000577735.1:c.318C>T
|
ENSP00000462491.1:p.Asp106=
|
|
NM_001165967.1:c.342C>T
|
NP_001159439.1:p.Asp114=
|
|
NM_032580.3:c.327C>T
|
NP_115969.2:p.Asp109=
|
|
XM_011524038.1:c.447C>T
|
XP_011522340.1:p.Asp149=
|
|
XM_011524039.1:c.438C>T
|
XP_011522341.1:p.Asp146=
|
|
XM_011524040.1:c.438C>T
|
XP_011522342.1:p.Asp146=
|
|
XM_011524041.1:c.429C>T
|
XP_011522343.1:p.Asp143=
|
|
XM_011524042.1:c.300C>T
|
XP_011522344.1:p.Asp100=
|
|
XR_934203.1:n.69+2108G>A
|
|
|
XM_017025232.1:c.447C>T
|
XP_016880721.1:p.Asp149=
|
|
XM_024451007.1:c.447C>T
|
XP_024306775.1:p.Asp149=
|
|
NM_001165967.2:c.342C>T
MANE Select
|
NP_001159439.1:p.Asp114=
|
|
NM_032580.4:c.327C>T
|
NP_115969.2:p.Asp109=
|
|