ENST00000682350.1:c.309C>T
|
ENSP00000508090.1:p.Ala103=
|
|
ENST00000682764.1:c.309C>T
|
ENSP00000506780.1:p.Ala103=
|
|
ENST00000339994.5:c.570C>T
MANE Select
|
ENSP00000345708.4:p.Ala190=
|
|
ENST00000339994.4:c.570C>T
|
ENSP00000345708.4:p.Ala190=
|
|
ENST00000526912.1:c.309C>T
|
ENSP00000432729.1:p.Ala103=
|
|
ENST00000528731.1:c.309C>T
|
ENSP00000434755.1:p.Ala103=
|
|
NM_000525.3:c.570C>T
|
NP_000516.3:p.Ala190=
|
|
NM_001166290.1:c.309C>T
|
NP_001159762.1:p.Ala103=
|
|
XM_006718226.2:c.309C>T
|
XP_006718289.1:p.Ala103=
|
|
XR_930867.1:n.728C>T
|
|
|
XM_006718226.3:c.309C>T
|
XP_006718289.1:p.Ala103=
|
|
XM_017017680.1:c.309C>T
|
XP_016873169.1:p.Ala103=
|
|
NM_001166290.2:c.309C>T
|
NP_001159762.1:p.Ala103=
|
|
NM_001377296.1:c.309C>T
|
NP_001364225.1:p.Ala103=
|
|
NM_001377297.1:c.309C>T
|
NP_001364226.1:p.Ala103=
|
|
NM_000525.4:c.570C>T
MANE Select
|
NP_000516.3:p.Ala190=
|
|