ENST00000697953.1:n.185A>T
|
|
|
ENST00000698016.1:c.156A>T
|
ENSP00000513502.1:p.Ala52=
|
|
ENST00000698022.1:c.114A>T
|
ENSP00000513504.1:p.Ala38=
|
|
ENST00000698027.1:c.156A>T
|
ENSP00000513505.1:p.Ala52=
|
|
ENST00000448276.7:c.297A>T
MANE Select
|
ENSP00000392617.2:p.Ala99=
|
|
ENST00000225742.13:c.72A>T
|
ENSP00000225742.9:p.Ala24=
|
|
ENST00000323347.14:c.153A>T
|
ENSP00000318451.10:p.Ala51=
|
|
ENST00000448276.6:c.297A>T
|
ENSP00000392617.2:p.Ala99=
|
|
ENST00000577686.1:n.53-308A>T
|
|
|
ENST00000580054.1:c.81A>T
|
ENSP00000463793.1:p.Ala27=
|
|
ENST00000584400.5:c.217-308A>T
|
ENSP00000464503.1:n.217-308A>T
|
|
ENST00000613943.4:c.186A>T
|
ENSP00000483605.1:p.Ala62=
|
|
NM_001098426.1:c.297A>T
|
NP_001091896.1:p.Ala99=
|
|
XM_005257604.2:c.72A>T
|
XP_005257661.2:p.Ala24=
|
|
NM_001330439.1:c.72A>T
|
NP_001317368.1:p.Ala24=
|
|
NM_001330440.1:c.153A>T
|
NP_001317369.1:p.Ala51=
|
|
NM_001098426.2:c.297A>T
MANE Select
|
NP_001091896.1:p.Ala99=
|
|
NM_001330440.2:c.153A>T
|
NP_001317369.1:p.Ala51=
|
|