ENST00000697953.1:n.187C>T
|
|
|
ENST00000698016.1:c.158C>T
|
ENSP00000513502.1:p.Ala53Val
|
|
ENST00000698022.1:c.116C>T
|
ENSP00000513504.1:p.Ala39Val
|
|
ENST00000698027.1:c.158C>T
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ENSP00000513505.1:p.Ala53Val
|
|
ENST00000448276.7:c.299C>T
MANE Select
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ENSP00000392617.2:p.Ala100Val
|
|
ENST00000225742.13:c.74C>T
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ENSP00000225742.9:p.Ala25Val
|
|
ENST00000323347.14:c.155C>T
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ENSP00000318451.10:p.Ala52Val
|
|
ENST00000448276.6:c.299C>T
|
ENSP00000392617.2:p.Ala100Val
|
|
ENST00000577686.1:n.53-306C>T
|
|
|
ENST00000580054.1:c.83C>T
|
ENSP00000463793.1:p.Ala28Val
|
|
ENST00000584400.5:c.217-306C>T
|
ENSP00000464503.1:n.217-306C>T
|
|
ENST00000613943.4:c.188C>T
|
ENSP00000483605.1:p.Ala63Val
|
|
NM_001098426.1:c.299C>T
|
NP_001091896.1:p.Ala100Val
|
|
XM_005257604.2:c.74C>T
|
XP_005257661.2:p.Ala25Val
|
|
NM_001330439.1:c.74C>T
|
NP_001317368.1:p.Ala25Val
|
|
NM_001330440.1:c.155C>T
|
NP_001317369.1:p.Ala52Val
|
|
NM_001098426.2:c.299C>T
MANE Select
|
NP_001091896.1:p.Ala100Val
|
|
NM_001330440.2:c.155C>T
|
NP_001317369.1:p.Ala52Val
|
|