ENST00000252288.8:c.486G>T
MANE Select
|
ENSP00000252288.1:p.Pro162=
|
|
ENST00000447102.8:c.486G>T
|
ENSP00000403536.2:p.Pro162=
|
|
ENST00000591788.3:c.169G>T
|
|
|
ENST00000640164.1:n.319G>T
|
|
|
ENST00000640762.1:c.417G>T
|
ENSP00000492031.1:p.Pro139=
|
|
ENST00000252288.6:c.486G>T
|
ENSP00000252288.1:p.Pro162=
|
|
ENST00000447102.7:c.486G>T
|
ENSP00000403536.2:p.Pro162=
|
|
ENST00000591788.2:c.171G>T
|
ENSP00000466341.2:p.Pro57=
|
|
NM_000156.5:c.486G>T
|
NP_000147.1:p.Pro162=
|
|
NM_138924.2:c.486G>T
|
NP_620279.1:p.Pro162=
|
|
NM_000156.6:c.486G>T
MANE Select
|
NP_000147.1:p.Pro162=
|
|
NM_138924.3:c.486G>T
|
NP_620279.1:p.Pro162=
|
|