ENST00000371117.8:c.10867C>G
MANE Select
|
ENSP00000360158.3:p.Pro3623Ala
|
|
ENST00000371117.7:c.10867C>G
|
ENSP00000360158.3:p.Pro3623Ala
|
|
NM_138694.3:c.10867C>G
|
NP_619639.3:p.Pro3623Ala
|
|
XM_011514679.1:c.10867C>G
|
XP_011512981.1:p.Pro3623Ala
|
|
XM_011514680.1:c.10867C>G
|
XP_011512982.1:p.Pro3623Ala
|
|
XM_011514681.1:c.10738C>G
|
XP_011512983.1:p.Pro3580Ala
|
|
XM_011514682.1:c.10729C>G
|
XP_011512984.1:p.Pro3577Ala
|
|
XM_011514683.1:c.10225C>G
|
XP_011512985.1:p.Pro3409Ala
|
|
XM_011514684.1:c.10156C>G
|
XP_011512986.1:p.Pro3386Ala
|
|
XM_011514687.1:c.10157-10039C>G
|
XP_011512989.1:n.10157-10039C>G
|
|
XM_011514690.1:c.4942C>G
|
XP_011512992.1:p.Pro1648Ala
|
|
XM_011514691.1:c.4942C>G
|
XP_011512993.1:p.Pro1648Ala
|
|
XR_926870.1:n.535+6886G>C
|
|
|
XR_926871.1:n.403+6886G>C
|
|
|
XR_926872.1:n.535+6886G>C
|
|
|
XM_011514680.3:c.10867C>G
|
XP_011512982.1:p.Pro3623Ala
|
|
XM_011514682.3:c.10729C>G
|
XP_011512984.1:p.Pro3577Ala
|
|
XM_011514683.3:c.10225C>G
|
XP_011512985.1:p.Pro3409Ala
|
|
XM_011514684.3:c.10156C>G
|
XP_011512986.1:p.Pro3386Ala
|
|
XM_011514690.3:c.4942C>G
|
XP_011512992.1:p.Pro1648Ala
|
|
XM_011514691.3:c.4942C>G
|
XP_011512993.1:p.Pro1648Ala
|
|
XM_017010944.2:c.10867C>G
|
XP_016866433.1:p.Pro3623Ala
|
|
XM_017010945.2:c.10792C>G
|
XP_016866434.1:p.Pro3598Ala
|
|
XM_017010946.2:c.10672C>G
|
XP_016866435.1:p.Pro3558Ala
|
|
XM_017010947.2:c.10603C>G
|
XP_016866436.1:p.Pro3535Ala
|
|
XM_017010948.2:c.10156C>G
|
XP_016866437.1:p.Pro3386Ala
|
|
XM_017010949.2:c.9007C>G
|
XP_016866438.1:p.Pro3003Ala
|
|
XR_001743469.1:n.11143C>G
|
|
|
XR_001744157.1:n.3145+6886G>C
|
|
|
XR_926870.2:n.3145+6886G>C
|
|
|
XR_926871.2:n.3013+6886G>C
|
|
|
XR_926872.2:n.3145+6886G>C
|
|
|
NM_138694.4:c.10867C>G
MANE Select
|
NP_619639.3:p.Pro3623Ala
|
|