ENST00000697953.1:n.181G>T
|
|
|
ENST00000698016.1:c.152G>T
|
ENSP00000513502.1:p.Gly51Val
|
|
ENST00000698022.1:c.110G>T
|
ENSP00000513504.1:p.Gly37Val
|
|
ENST00000698027.1:c.152G>T
|
ENSP00000513505.1:p.Gly51Val
|
|
ENST00000448276.7:c.293G>T
MANE Select
|
ENSP00000392617.2:p.Gly98Val
|
|
ENST00000225742.13:c.68G>T
|
ENSP00000225742.9:p.Gly23Val
|
|
ENST00000323347.14:c.149G>T
|
ENSP00000318451.10:p.Gly50Val
|
|
ENST00000448276.6:c.293G>T
|
ENSP00000392617.2:p.Gly98Val
|
|
ENST00000577686.1:n.53-312G>T
|
|
|
ENST00000580054.1:c.77G>T
|
ENSP00000463793.1:p.Gly26Val
|
|
ENST00000584400.5:c.217-312G>T
|
ENSP00000464503.1:n.217-312G>T
|
|
ENST00000613943.4:c.182G>T
|
ENSP00000483605.1:p.Gly61Val
|
|
NM_001098426.1:c.293G>T
|
NP_001091896.1:p.Gly98Val
|
|
XM_005257604.2:c.68G>T
|
XP_005257661.2:p.Gly23Val
|
|
NM_001330439.1:c.68G>T
|
NP_001317368.1:p.Gly23Val
|
|
NM_001330440.1:c.149G>T
|
NP_001317369.1:p.Gly50Val
|
|
NM_001098426.2:c.293G>T
MANE Select
|
NP_001091896.1:p.Gly98Val
|
|
NM_001330440.2:c.149G>T
|
NP_001317369.1:p.Gly50Val
|
|