ENST00000697602.1:n.1428G=
|
|
|
ENST00000697603.1:c.3532G=
|
ENSP00000513358.1:p.Asp1178=
|
|
ENST00000314191.7:c.10855G=
MANE Select
|
ENSP00000313420.3:p.Asp3619=
|
|
ENST00000314191.6:c.10855G=
|
ENSP00000313420.3:p.Asp3619=
|
|
ENST00000338368.7:c.10855G=
|
ENSP00000345182.4:p.Asp3619=
|
|
NM_001081640.1:c.10855G=
|
NP_001075109.1:p.Asp3619=
|
|
NM_006904.6:c.10855G= , LRG_162t1:c.10855G=
|
NP_008835.5:p.Asp3619=
|
|
XM_011517567.1:c.10858G=
|
XP_011515869.1:p.Asp3620=
|
|
XM_011517568.1:c.10858G=
|
XP_011515870.1:p.Asp3620=
|
|
NM_001081640.2:c.10855G=
|
NP_001075109.1:p.Asp3619=
|
|
NM_006904.7:c.10855G=
MANE Select
|
NP_008835.5:p.Asp3619=
|
|