ENST00000333213.11:c.569T>C
MANE Select
|
ENSP00000327487.6:p.Val190Ala
|
|
ENST00000434205.8:c.266T>C
|
ENSP00000406559.4:p.Val89Ala
|
|
ENST00000545228.3:c.569T>C
|
ENSP00000438169.3:p.Val190Ala
|
|
ENST00000579449.2:n.368T>C
|
|
|
ENST00000580013.6:n.578T>C
|
|
|
ENST00000583818.2:c.623T>C
|
ENSP00000461928.2:n.623T>C
|
|
ENST00000679370.1:n.956T>C
|
|
|
ENST00000679429.1:c.*27T>C
|
ENSP00000505403.1:n.*27T>C
|
|
ENST00000679443.1:n.444T>C
|
|
|
ENST00000679782.1:c.569T>C
|
ENSP00000505995.1:p.Val190Ala
|
|
ENST00000679919.1:n.444T>C
|
|
|
ENST00000679928.1:c.*180T>C
|
ENSP00000506071.1:n.*180T>C
|
|
ENST00000680528.1:n.594T>C
|
|
|
ENST00000680999.1:c.569T>C
|
ENSP00000504984.1:p.Val190Ala
|
|
ENST00000681282.1:c.569T>C
|
ENSP00000506339.1:p.Val190Ala
|
|
ENST00000333213.10:c.569T>C
|
ENSP00000327487.6:p.Val190Ala
|
|
ENST00000578415.1:c.529T>C
|
|
|
ENST00000583173.5:c.404T>C
|
ENSP00000463619.1:p.Val135Ala
|
|
ENST00000583818.1:c.518T>C
|
ENSP00000461928.1:n.518T>C
|
|
NM_207346.2:c.569T>C
|
NP_997229.2:p.Val190Ala
|
|
XM_005257229.2:c.569T>C
|
XP_005257286.1:p.Val190Ala
|
|
XM_006721821.2:c.266T>C
|
XP_006721884.1:p.Val89Ala
|
|
XM_011524616.1:c.569T>C
|
XP_011522918.1:p.Val190Ala
|
|
XM_011524617.1:c.569T>C
|
XP_011522919.1:p.Val190Ala
|
|
XM_011524618.1:c.569T>C
|
XP_011522920.1:p.Val190Ala
|
|
XR_243646.2:n.599T>C
|
|
|
XM_005257229.4:c.569T>C
|
XP_005257286.1:p.Val190Ala
|
|
XR_243646.4:n.605T>C
|
|
|
NM_207346.3:c.569T>C
MANE Select
|
NP_997229.2:p.Val190Ala
|
|