ENST00000301608.9:c.913G=
|
ENSP00000301608.4:p.Ala305=
|
|
ENST00000293217.10:c.913G=
MANE Select
|
ENSP00000293217.4:p.Ala305=
|
|
ENST00000293217.9:c.913G=
|
ENSP00000293217.4:p.Ala305=
|
|
ENST00000301608.8:c.913G=
|
ENSP00000301608.4:p.Ala305=
|
|
ENST00000572047.5:c.1087G=
|
ENSP00000459936.1:n.1087G=
|
|
ENST00000573078.5:c.*402G=
|
ENSP00000458325.1:n.*402G=
|
|
ENST00000589744.1:n.163G=
|
|
|
NM_001185039.1:c.799G=
|
NP_001171968.1:p.Ala267=
|
|
NM_004035.6:c.913G=
|
NP_004026.2:p.Ala305=
|
|
NM_007292.5:c.913G=
|
NP_009223.2:p.Ala305=
|
|
XM_011524868.1:c.709G=
|
XP_011523170.1:p.Ala237=
|
|
XM_011524869.1:c.505G=
|
XP_011523171.1:p.Ala169=
|
|
XM_011524868.3:c.709G=
|
XP_011523170.1:p.Ala237=
|
|
XM_011524869.3:c.505G=
|
XP_011523171.1:p.Ala169=
|
|
NM_004035.7:c.913G=
MANE Select
|
NP_004026.2:p.Ala305=
|
|
NM_001185039.2:c.799G=
|
NP_001171968.1:p.Ala267=
|
|
NM_007292.6:c.913G=
|
NP_009223.2:p.Ala305=
|
|