ENST00000264380.9:c.3490C>G
MANE Select
|
ENSP00000264380.4:p.Pro1164Ala
|
|
ENST00000264380.8:c.3490C>G
|
ENSP00000264380.4:p.Pro1164Ala
|
|
ENST00000452564.1:c.3322C>G
|
ENSP00000405736.1:p.Pro1108Ala
|
|
NM_015040.3:c.3490C>G
|
NP_055855.2:p.Pro1164Ala
|
|
XM_011510778.1:c.3526C>G
|
XP_011509080.1:p.Pro1176Ala
|
|
XM_011510779.1:c.3526C>G
|
XP_011509081.1:p.Pro1176Ala
|
|
XM_011510780.1:c.3523C>G
|
XP_011509082.1:p.Pro1175Ala
|
|
XM_011510781.1:c.3508C>G
|
XP_011509083.1:p.Pro1170Ala
|
|
XM_011510782.1:c.3526C>G
|
XP_011509084.1:p.Pro1176Ala
|
|
XM_011510783.1:c.3358C>G
|
XP_011509085.1:p.Pro1120Ala
|
|
XM_011510784.1:c.3355C>G
|
XP_011509086.1:p.Pro1119Ala
|
|
XM_011510785.1:c.3340C>G
|
XP_011509087.1:p.Pro1114Ala
|
|
XM_011510786.1:c.3235C>G
|
XP_011509088.1:p.Pro1079Ala
|
|
XM_011510787.1:c.3232C>G
|
XP_011509089.1:p.Pro1078Ala
|
|
XM_011510788.1:c.3199C>G
|
XP_011509090.1:p.Pro1067Ala
|
|
XM_011510789.1:c.3049C>G
|
XP_011509091.1:p.Pro1017Ala
|
|
XM_011510790.1:c.2533C>G
|
XP_011509092.1:p.Pro845Ala
|
|
XM_011510791.1:c.2533C>G
|
XP_011509093.1:p.Pro845Ala
|
|
XM_011510792.1:c.3526C>G
|
XP_011509094.1:p.Pro1176Ala
|
|
XR_922888.1:n.3663C>G
|
|
|
XM_011510778.3:c.3526C>G
|
XP_011509080.1:p.Pro1176Ala
|
|
XM_011510779.2:c.3526C>G
|
XP_011509081.1:p.Pro1176Ala
|
|
XM_011510780.2:c.3523C>G
|
XP_011509082.1:p.Pro1175Ala
|
|
XM_011510781.3:c.3508C>G
|
XP_011509083.1:p.Pro1170Ala
|
|
XM_011510782.3:c.3526C>G
|
XP_011509084.1:p.Pro1176Ala
|
|
XM_011510783.3:c.3358C>G
|
XP_011509085.1:p.Pro1120Ala
|
|
XM_011510784.2:c.3355C>G
|
XP_011509086.1:p.Pro1119Ala
|
|
XM_011510785.3:c.3340C>G
|
XP_011509087.1:p.Pro1114Ala
|
|
XM_011510786.3:c.3235C>G
|
XP_011509088.1:p.Pro1079Ala
|
|
XM_011510789.2:c.3049C>G
|
XP_011509091.1:p.Pro1017Ala
|
|
XM_011510792.3:c.3526C>G
|
XP_011509094.1:p.Pro1176Ala
|
|
XM_017003568.1:c.3472C>G
|
XP_016859057.1:p.Pro1158Ala
|
|
XM_017003569.1:c.3304C>G
|
XP_016859058.1:p.Pro1102Ala
|
|
XM_017003570.1:c.3031C>G
|
XP_016859059.1:p.Pro1011Ala
|
|
XM_017003571.1:c.2881C>G
|
XP_016859060.1:p.Pro961Ala
|
|
XM_017003572.1:c.2533C>G
|
XP_016859061.1:p.Pro845Ala
|
|
XM_017003573.1:c.2533C>G
|
XP_016859062.1:p.Pro845Ala
|
|
XM_017003574.1:c.2533C>G
|
XP_016859063.1:p.Pro845Ala
|
|
NM_015040.4:c.3490C>G
MANE Select
|
NP_055855.2:p.Pro1164Ala
|
|