|
ENST00000700029.2:c.1009A>G
|
ENSP00000514759.2:p.Ile337Val
|
|
|
ENST00000710265.1:c.916A>G
|
ENSP00000518161.1:p.Ile306Val
|
|
|
ENST00000472832.3:c.916A>G
|
ENSP00000483066.2:p.Ile306Val
|
|
|
ENST00000688158.2:n.1651A>G
|
|
|
|
ENST00000688922.2:c.*746A>G
|
ENSP00000508742.2:n.*746A>G
|
|
|
ENST00000700021.1:c.871A>G
|
ENSP00000514757.1:p.Ile291Val
|
|
|
ENST00000700022.1:c.*255A>G
|
ENSP00000514758.1:n.*255A>G
|
|
|
ENST00000700023.1:n.2074A>G
|
|
|
|
ENST00000700024.1:n.2308A>G
|
|
|
|
ENST00000700025.1:n.1685A>G
|
|
|
|
ENST00000700026.1:n.553A>G
|
|
|
|
ENST00000706954.1:c.916A>G
|
ENSP00000516674.1:p.Ile306Val
|
|
|
ENST00000706955.1:c.*951A>G
|
ENSP00000516675.1:n.*951A>G
|
|
|
ENST00000686459.1:c.*502A>G
|
ENSP00000508909.1:n.*502A>G
|
|
|
ENST00000688158.1:c.*1027A>G
|
ENSP00000509254.1:n.*1027A>G
|
|
|
ENST00000688308.1:c.916A>G
|
ENSP00000508752.1:p.Ile306Val
|
|
|
ENST00000688922.1:c.837A>G
|
|
|
|
ENST00000693560.1:c.1435A>G
|
ENSP00000509861.1:p.Ile479Val
|
|
|
ENST00000371953.8:c.916A>G
MANE Select
|
ENSP00000361021.3:p.Ile306Val
|
|
|
ENST00000371953.7:c.916A>G
|
ENSP00000361021.3:p.Ile306Val
|
|
|
ENST00000472832.2:c.343A>G
|
ENSP00000483066.1:p.Ile115Val
|
|
|
NM_000314.5:c.916A>G
|
NP_000305.3:p.Ile306Val
|
|
|
NM_000314.6:c.916A>G
|
NP_000305.3:p.Ile306Val
|
|
|
NM_001304717.2:c.1435A>G
|
NP_001291646.2:p.Ile479Val
|
|
|
NM_001304718.1:c.325A>G
|
NP_001291647.1:p.Ile109Val
|
|
|
XM_006717926.2:c.871A>G
|
XP_006717989.1:p.Ile291Val
|
|
|
XM_011539981.1:c.916A>G
|
XP_011538283.1:p.Ile306Val
|
|
|
XM_011539982.1:c.820A>G
|
XP_011538284.1:p.Ile274Val
|
|
|
XR_945791.1:n.1486A>G
|
|
|
|
NM_000314.7:c.916A>G
|
NP_000305.3:p.Ile306Val
|
|
|
NM_001304717.5:c.1435A>G
|
NP_001291646.4:p.Ile479Val
|
|
|
NM_001304718.2:c.325A>G
|
NP_001291647.1:p.Ile109Val
|
|
|
NM_000314.8:c.916A>G
MANE Select
|
NP_000305.3:p.Ile306Val
|
|
