ENST00000326003.7:c.757A=
MANE Select
|
ENSP00000314151.1:p.Ile253=
|
|
ENST00000326003.6:c.757A=
|
ENSP00000314151.1:p.Ile253=
|
|
ENST00000360617.7:c.1199A=
|
ENSP00000353829.2:n.1199A=
|
|
ENST00000422986.6:c.*413A=
|
ENSP00000393628.2:n.*413A=
|
|
ENST00000595392.5:c.*258A=
|
ENSP00000468912.1:n.*258A=
|
|
ENST00000595952.5:c.628A=
|
ENSP00000471155.1:p.Ile210=
|
|
ENST00000596333.1:n.935A=
|
|
|
ENST00000598145.1:c.759A=
|
|
|
ENST00000601349.5:n.2036A=
|
|
|
ENST00000601812.1:n.1189A=
|
|
|
ENST00000617027.4:c.634A=
|
ENSP00000483513.1:p.Ile212=
|
|
NM_001030047.1:c.*482A=
|
NP_001025218.1:n.*482A=
|
|
NM_001030048.1:c.628A=
|
NP_001025219.1:p.Ile210=
|
|
NM_001648.2:c.757A=
MANE Select
|
NP_001639.1:p.Ile253=
|
|
XM_011526923.1:c.775A=
|
XP_011525225.1:p.Ile259=
|
|
XR_935817.1:n.1324+844A=
|
|
|