ENST00000697953.1:n.226A>T
|
|
|
ENST00000698016.1:c.197A>T
|
ENSP00000513502.1:p.Asp66Val
|
|
ENST00000698021.1:c.1A>T
|
|
|
ENST00000698022.1:c.155A>T
|
ENSP00000513504.1:p.Asp52Val
|
|
ENST00000698027.1:c.197A>T
|
ENSP00000513505.1:p.Asp66Val
|
|
ENST00000448276.7:c.338A>T
MANE Select
|
ENSP00000392617.2:p.Asp113Val
|
|
ENST00000225742.13:c.113A>T
|
ENSP00000225742.9:p.Asp38Val
|
|
ENST00000323347.14:c.194A>T
|
ENSP00000318451.10:p.Asp65Val
|
|
ENST00000448276.6:c.338A>T
|
ENSP00000392617.2:p.Asp113Val
|
|
ENST00000577686.1:n.53-267A>T
|
|
|
ENST00000580054.1:c.122A>T
|
ENSP00000463793.1:p.Asp41Val
|
|
ENST00000584400.5:c.217-267A>T
|
ENSP00000464503.1:n.217-267A>T
|
|
ENST00000613943.4:c.227A>T
|
ENSP00000483605.1:p.Asp76Val
|
|
NM_001098426.1:c.338A>T
|
NP_001091896.1:p.Asp113Val
|
|
XM_005257604.2:c.113A>T
|
XP_005257661.2:p.Asp38Val
|
|
NM_001330439.1:c.113A>T
|
NP_001317368.1:p.Asp38Val
|
|
NM_001330440.1:c.194A>T
|
NP_001317369.1:p.Asp65Val
|
|
NM_001098426.2:c.338A>T
MANE Select
|
NP_001091896.1:p.Asp113Val
|
|
NM_001330440.2:c.194A>T
|
NP_001317369.1:p.Asp65Val
|
|