ENST00000373674.4:c.56T>A
MANE Select
|
ENSP00000362778.3:p.Val19Glu
|
|
ENST00000647861.1:c.56T>A
|
ENSP00000497550.1:p.Val19Glu
|
|
ENST00000373674.3:c.56T>A
|
ENSP00000362778.3:p.Val19Glu
|
|
ENST00000611814.4:c.56T>A
|
ENSP00000478888.1:p.Val19Glu
|
|
NM_001199159.1:c.56T>A
|
NP_001186088.1:p.Val19Glu
|
|
NM_153370.2:c.56T>A
|
NP_699201.2:p.Val19Glu
|
|
XM_005248917.1:c.56T>A
|
XP_005248974.1:p.Val19Glu
|
|
XM_011514375.1:c.56T>A
|
XP_011512677.1:p.Val19Glu
|
|
XM_005248917.3:c.56T>A
|
XP_005248974.1:p.Val19Glu
|
|
XM_011514375.3:c.56T>A
|
XP_011512677.1:p.Val19Glu
|
|
XM_017010430.2:c.56T>A
|
XP_016865919.1:p.Val19Glu
|
|
NM_153370.3:c.56T>A
MANE Select
|
NP_699201.2:p.Val19Glu
|
|
NM_001199159.2:c.56T>A
|
NP_001186088.1:p.Val19Glu
|
|