ENST00000298910.12:c.4265G>T
MANE Select
|
ENSP00000298910.7:p.Ser1422Ile
|
|
ENST00000679360.1:c.*3174G>T
|
ENSP00000505368.1:n.*3174G>T
|
|
ENST00000680790.1:c.4010G>T
|
ENSP00000505335.1:p.Ser1337Ile
|
|
ENST00000298910.11:c.4265G>T
|
ENSP00000298910.7:p.Ser1422Ile
|
|
ENST00000430804.5:c.1561G>T
|
|
|
ENST00000479187.5:n.946G>T
|
|
|
NM_198578.3:c.4265G>T
|
NP_940980.3:p.Ser1422Ile
|
|
XM_005268629.2:c.4265G>T
|
XP_005268686.1:p.Ser1422Ile
|
|
XM_011537877.1:c.4265G>T
|
XP_011536179.1:p.Ser1422Ile
|
|
XM_011537878.1:c.4265G>T
|
XP_011536180.1:p.Ser1422Ile
|
|
XM_011537879.1:c.3062G>T
|
XP_011536181.1:p.Ser1021Ile
|
|
XM_011537880.1:c.4265G>T
|
XP_011536182.1:p.Ser1422Ile
|
|
XM_011537881.1:c.4265G>T
|
XP_011536183.1:p.Ser1422Ile
|
|
XM_005268629.4:c.4265G>T
|
XP_005268686.1:p.Ser1422Ile
|
|
XM_011537877.3:c.4265G>T
|
XP_011536179.1:p.Ser1422Ile
|
|
XM_011537881.3:c.4265G>T
|
XP_011536183.1:p.Ser1422Ile
|
|
XM_017018786.2:c.4265G>T
|
XP_016874275.1:p.Ser1422Ile
|
|
XM_017018787.1:c.1181G>T
|
XP_016874276.1:p.Ser394Ile
|
|
XM_017018788.2:c.527G>T
|
XP_016874277.1:p.Ser176Ile
|
|
XM_024448833.1:c.3062G>T
|
XP_024304601.1:p.Ser1021Ile
|
|
XR_001748574.2:n.4507G>T
|
|
|
NM_198578.4:c.4265G>T
MANE Select
|
NP_940980.4:p.Ser1422Ile
|
|