ENST00000697953.1:n.207A>G
|
|
|
ENST00000698016.1:c.178A>G
|
ENSP00000513502.1:p.Met60Val
|
|
ENST00000698022.1:c.136A>G
|
ENSP00000513504.1:p.Met46Val
|
|
ENST00000698027.1:c.178A>G
|
ENSP00000513505.1:p.Met60Val
|
|
ENST00000448276.7:c.319A>G
MANE Select
|
ENSP00000392617.2:p.Met107Val
|
|
ENST00000225742.13:c.94A>G
|
ENSP00000225742.9:p.Met32Val
|
|
ENST00000323347.14:c.175A>G
|
ENSP00000318451.10:p.Met59Val
|
|
ENST00000448276.6:c.319A>G
|
ENSP00000392617.2:p.Met107Val
|
|
ENST00000577686.1:n.53-286A>G
|
|
|
ENST00000580054.1:c.103A>G
|
ENSP00000463793.1:p.Met35Val
|
|
ENST00000584400.5:c.217-286A>G
|
ENSP00000464503.1:n.217-286A>G
|
|
ENST00000613943.4:c.208A>G
|
ENSP00000483605.1:p.Met70Val
|
|
NM_001098426.1:c.319A>G
|
NP_001091896.1:p.Met107Val
|
|
XM_005257604.2:c.94A>G
|
XP_005257661.2:p.Met32Val
|
|
NM_001330439.1:c.94A>G
|
NP_001317368.1:p.Met32Val
|
|
NM_001330440.1:c.175A>G
|
NP_001317369.1:p.Met59Val
|
|
NM_001098426.2:c.319A>G
MANE Select
|
NP_001091896.1:p.Met107Val
|
|
NM_001330440.2:c.175A>G
|
NP_001317369.1:p.Met59Val
|
|