ENST00000697953.1:n.278C>A
|
|
|
ENST00000698015.1:n.24C>A
|
|
|
ENST00000698016.1:c.249C>A
|
ENSP00000513502.1:p.Ala83=
|
|
ENST00000698021.1:c.53C>A
|
|
|
ENST00000698022.1:c.207C>A
|
ENSP00000513504.1:p.Ala69=
|
|
ENST00000698027.1:c.249C>A
|
ENSP00000513505.1:p.Ala83=
|
|
ENST00000448276.7:c.390C>A
MANE Select
|
ENSP00000392617.2:p.Ala130=
|
|
ENST00000225742.13:c.165C>A
|
ENSP00000225742.9:p.Ala55=
|
|
ENST00000323347.14:c.246C>A
|
ENSP00000318451.10:p.Ala82=
|
|
ENST00000448276.6:c.390C>A
|
ENSP00000392617.2:p.Ala130=
|
|
ENST00000577686.1:n.53-215C>A
|
|
|
ENST00000580054.1:c.174C>A
|
ENSP00000463793.1:p.Ala58=
|
|
ENST00000584400.5:c.217-215C>A
|
ENSP00000464503.1:n.217-215C>A
|
|
ENST00000613943.4:c.279C>A
|
ENSP00000483605.1:p.Ala93=
|
|
NM_001098426.1:c.390C>A
|
NP_001091896.1:p.Ala130=
|
|
XM_005257604.2:c.165C>A
|
XP_005257661.2:p.Ala55=
|
|
NM_001330439.1:c.165C>A
|
NP_001317368.1:p.Ala55=
|
|
NM_001330440.1:c.246C>A
|
NP_001317369.1:p.Ala82=
|
|
NM_001098426.2:c.390C>A
MANE Select
|
NP_001091896.1:p.Ala130=
|
|
NM_001330440.2:c.246C>A
|
NP_001317369.1:p.Ala82=
|
|