ENST00000697953.1:n.112G>T
|
|
|
ENST00000698016.1:c.83G>T
|
ENSP00000513502.1:p.Gly28Val
|
|
ENST00000698022.1:c.41G>T
|
ENSP00000513504.1:p.Gly14Val
|
|
ENST00000698027.1:c.83G>T
|
ENSP00000513505.1:p.Gly28Val
|
|
ENST00000448276.7:c.224G>T
MANE Select
|
ENSP00000392617.2:p.Gly75Val
|
|
ENST00000225742.13:c.-2G>T
|
ENSP00000225742.9:n.-2G>T
|
|
ENST00000323347.14:c.80G>T
|
ENSP00000318451.10:p.Gly27Val
|
|
ENST00000448276.6:c.224G>T
|
ENSP00000392617.2:p.Gly75Val
|
|
ENST00000577686.1:n.53-381G>T
|
|
|
ENST00000580054.1:c.8G>T
|
ENSP00000463793.1:p.Gly3Val
|
|
ENST00000584400.5:c.217-381G>T
|
ENSP00000464503.1:n.217-381G>T
|
|
ENST00000613943.4:c.113G>T
|
ENSP00000483605.1:p.Gly38Val
|
|
NM_001098426.1:c.224G>T
|
NP_001091896.1:p.Gly75Val
|
|
XM_005257604.2:c.-2G>T
|
XP_005257661.2:n.-2G>T
|
|
NM_001330439.1:c.-2G>T
|
NP_001317368.1:n.-2G>T
|
|
NM_001330440.1:c.80G>T
|
NP_001317369.1:p.Gly27Val
|
|
NM_001098426.2:c.224G>T
MANE Select
|
NP_001091896.1:p.Gly75Val
|
|
NM_001330440.2:c.80G>T
|
NP_001317369.1:p.Gly27Val
|
|