ENST00000418386.3:c.189T>A
MANE Select
|
ENSP00000413450.2:p.Pro63=
|
|
ENST00000418386.2:c.189T>A
|
ENSP00000413450.2:p.Pro63=
|
|
ENST00000454783.5:c.189T>A
|
ENSP00000403495.1:p.Pro63=
|
|
ENST00000471842.1:n.437T>A
|
|
|
ENST00000489638.5:n.317T>A
|
|
|
NM_000595.3:c.189T>A
|
NP_000586.2:p.Pro63=
|
|
NM_001159740.2:c.189T>A
|
NP_001153212.1:p.Pro63=
|
|
XM_011514614.1:c.189T>A
|
XP_011512916.1:p.Pro63=
|
|
XM_011514615.1:c.189T>A
|
XP_011512917.1:p.Pro63=
|
|
XM_011514616.1:c.189T>A
|
XP_011512918.1:p.Pro63=
|
|
XM_011514617.1:c.189T>A
|
XP_011512919.1:p.Pro63=
|
|
XM_011514618.1:c.189T>A
|
XP_011512920.1:p.Pro63=
|
|
XM_011514615.2:c.189T>A
|
XP_011512917.1:p.Pro63=
|
|
XM_011514616.2:c.189T>A
|
XP_011512918.1:p.Pro63=
|
|
XM_011514617.2:c.189T>A
|
XP_011512919.1:p.Pro63=
|
|
NM_000595.4:c.189T>A
MANE Select
|
NP_000586.2:p.Pro63=
|
|