ENST00000247933.9:c.770A=
|
ENSP00000247933.4:p.Asp257=
|
|
ENST00000514224.2:c.770A=
MANE Select
|
ENSP00000425081.2:p.Asp257=
|
|
ENST00000652070.1:n.826A=
|
|
|
ENST00000247933.8:c.770A=
|
ENSP00000247933.4:p.Asp257=
|
|
ENST00000502910.5:c.629A=
|
ENSP00000422952.1:p.Asp210=
|
|
ENST00000514192.5:c.587A=
|
ENSP00000423685.1:p.Asp196=
|
|
ENST00000514224.1:c.374A=
|
ENSP00000425081.1:p.Asp125=
|
|
ENST00000514698.5:n.670A=
|
|
|
NM_000203.4:c.770A=
|
NP_000194.2:p.Asp257=
|
|
NR_110313.1:n.858A=
|
|
|
XM_006713882.2:c.374A=
|
XP_006713945.1:p.Asp125=
|
|
XM_011513459.1:c.629A=
|
XP_011511761.1:p.Asp210=
|
|
XM_011513460.1:c.629A=
|
XP_011511762.1:p.Asp210=
|
|
XM_011513461.1:c.563A=
|
XP_011511763.1:p.Asp188=
|
|
XM_011513462.1:c.482A=
|
XP_011511764.1:p.Asp161=
|
|
XM_011513463.1:c.482A=
|
XP_011511765.1:p.Asp161=
|
|
XR_924947.1:n.839A=
|
|
|
NM_000203.5:c.770A=
MANE Select
|
NP_000194.2:p.Asp257=
|
|
NM_001363576.1:c.374A=
|
NP_001350505.1:p.Asp125=
|
|
XM_011513461.2:c.563A=
|
XP_011511763.1:p.Asp188=
|
|
XM_017008163.1:c.-191A=
|
XP_016863652.1:n.-191A=
|
|