ENST00000373631.8:c.3726T>G
MANE Select
|
ENSP00000362734.3:p.Leu1242=
|
|
ENST00000373631.7:c.3726T>G
|
ENSP00000362734.3:p.Leu1242=
|
|
ENST00000460253.1:c.2730T>G
|
ENSP00000435279.1:p.Leu910=
|
|
NM_173689.6:c.3726T>G
|
NP_775960.4:p.Leu1242=
|
|
NR_104603.1:n.2840T>G
|
|
|
XM_005251934.1:c.2730T>G
|
XP_005251991.1:p.Leu910=
|
|
XM_011518556.1:c.3699T>G
|
XP_011516858.1:p.Leu1233=
|
|
XM_011518557.1:c.3531T>G
|
XP_011516859.1:p.Leu1177=
|
|
XM_011518558.1:c.3531T>G
|
XP_011516860.1:p.Leu1177=
|
|
XM_005251934.3:c.2730T>G
|
XP_005251991.1:p.Leu910=
|
|
XM_011518556.3:c.3699T>G
|
XP_011516858.1:p.Leu1233=
|
|
XM_011518557.3:c.3531T>G
|
XP_011516859.1:p.Leu1177=
|
|
XM_011518558.3:c.3531T>G
|
XP_011516860.1:p.Leu1177=
|
|
NM_173689.7:c.3726T>G
MANE Select
|
NP_775960.4:p.Leu1242=
|
|
NR_104603.2:n.2840T>G
|
|
|