ENST00000697953.1:n.275T>G
|
|
|
ENST00000698015.1:n.21T>G
|
|
|
ENST00000698016.1:c.246T>G
|
ENSP00000513502.1:p.Pro82=
|
|
ENST00000698021.1:c.50T>G
|
|
|
ENST00000698022.1:c.204T>G
|
ENSP00000513504.1:p.Pro68=
|
|
ENST00000698027.1:c.246T>G
|
ENSP00000513505.1:p.Pro82=
|
|
ENST00000448276.7:c.387T>G
MANE Select
|
ENSP00000392617.2:p.Pro129=
|
|
ENST00000225742.13:c.162T>G
|
ENSP00000225742.9:p.Pro54=
|
|
ENST00000323347.14:c.243T>G
|
ENSP00000318451.10:p.Pro81=
|
|
ENST00000448276.6:c.387T>G
|
ENSP00000392617.2:p.Pro129=
|
|
ENST00000577686.1:n.53-218T>G
|
|
|
ENST00000580054.1:c.171T>G
|
ENSP00000463793.1:p.Pro57=
|
|
ENST00000584400.5:c.217-218T>G
|
ENSP00000464503.1:n.217-218T>G
|
|
ENST00000613943.4:c.276T>G
|
ENSP00000483605.1:p.Pro92=
|
|
NM_001098426.1:c.387T>G
|
NP_001091896.1:p.Pro129=
|
|
XM_005257604.2:c.162T>G
|
XP_005257661.2:p.Pro54=
|
|
NM_001330439.1:c.162T>G
|
NP_001317368.1:p.Pro54=
|
|
NM_001330440.1:c.243T>G
|
NP_001317369.1:p.Pro81=
|
|
NM_001098426.2:c.387T>G
MANE Select
|
NP_001091896.1:p.Pro129=
|
|
NM_001330440.2:c.243T>G
|
NP_001317369.1:p.Pro81=
|
|