ENST00000309041.12:c.1991A>G
|
ENSP00000308021.8:p.Asp664Gly
|
|
ENST00000547926.7:c.1909+617A>G
|
ENSP00000448573.3:n.1909+617A>G
|
|
ENST00000552810.6:c.1991A>G
MANE Select
|
ENSP00000448012.1:p.Asp664Gly
|
|
ENST00000671822.2:n.3547A>G
|
|
|
ENST00000672414.2:c.*162A>G
|
ENSP00000500729.1:n.*162A>G
|
|
ENST00000673058.2:c.1991A>G
|
ENSP00000500665.2:p.Asp664Gly
|
|
ENST00000674971.1:c.1991A>G
|
ENSP00000502194.1:p.Asp664Gly
|
|
ENST00000675230.1:c.1970A>G
|
ENSP00000502503.1:p.Asp657Gly
|
|
ENST00000675408.1:c.1991A>G
|
ENSP00000502298.1:p.Asp664Gly
|
|
ENST00000675476.1:c.2852A>G
|
ENSP00000502161.1:p.Asp951Gly
|
|
ENST00000675628.1:n.2218A>G
|
|
|
ENST00000675794.1:c.*162A>G
|
ENSP00000502841.1:n.*162A>G
|
|
ENST00000675833.1:c.2759A>G
|
ENSP00000502559.1:p.Asp920Gly
|
|
ENST00000676074.1:c.1991A>G
|
ENSP00000502079.1:p.Asp664Gly
|
|
ENST00000676363.1:n.4054A>G
|
|
|
ENST00000676448.1:c.1909+617A>G
|
ENSP00000501987.1:n.1909+617A>G
|
|
ENST00000309041.11:c.1997A>G
|
ENSP00000308021.7:p.Asp666Gly
|
|
ENST00000397838.7:c.1997A>G
|
ENSP00000380938.4:p.Asp666Gly
|
|
ENST00000547926.6:c.1807+617A>G
|
ENSP00000448573.2:n.1807+617A>G
|
|
ENST00000552810.5:c.1991A>G
|
ENSP00000448012.1:p.Asp664Gly
|
|
ENST00000604024.5:c.1250A>G
|
ENSP00000473863.1:p.Asp417Gly
|
|
NM_025114.3:c.1991A>G
|
NP_079390.3:p.Asp664Gly
|
|
XM_011538756.1:c.2852A>G
|
XP_011537058.1:p.Asp951Gly
|
|
XM_011538757.1:c.2852A>G
|
XP_011537059.1:p.Asp951Gly
|
|
XM_011538758.1:c.2852A>G
|
XP_011537060.1:p.Asp951Gly
|
|
XM_011538759.1:c.2852A>G
|
XP_011537061.1:p.Asp951Gly
|
|
XM_011538760.1:c.2852A>G
|
XP_011537062.1:p.Asp951Gly
|
|
XM_011538761.1:c.2852A>G
|
XP_011537063.1:p.Asp951Gly
|
|
XM_011538762.1:c.2084A>G
|
XP_011537064.1:p.Asp695Gly
|
|
XM_011538763.1:c.1991A>G
|
XP_011537065.1:p.Asp664Gly
|
|
XM_011538764.1:c.2852A>G
|
XP_011537066.1:p.Asp951Gly
|
|
XM_011538765.1:c.2852A>G
|
XP_011537067.1:p.Asp951Gly
|
|
XM_011538766.1:c.1313A>G
|
XP_011537068.1:p.Asp438Gly
|
|
XM_011538756.3:c.2852A>G
|
XP_011537058.1:p.Asp951Gly
|
|
XM_011538757.3:c.2852A>G
|
XP_011537059.1:p.Asp951Gly
|
|
XM_011538758.3:c.2852A>G
|
XP_011537060.1:p.Asp951Gly
|
|
XM_011538759.2:c.2852A>G
|
XP_011537061.1:p.Asp951Gly
|
|
XM_011538760.2:c.2852A>G
|
XP_011537062.1:p.Asp951Gly
|
|
XM_011538761.2:c.2852A>G
|
XP_011537063.1:p.Asp951Gly
|
|
XM_011538762.3:c.2084A>G
|
XP_011537064.1:p.Asp695Gly
|
|
XM_011538763.3:c.1991A>G
|
XP_011537065.1:p.Asp664Gly
|
|
XM_011538764.3:c.2852A>G
|
XP_011537066.1:p.Asp951Gly
|
|
XM_011538765.3:c.2852A>G
|
XP_011537067.1:p.Asp951Gly
|
|
XM_011538766.3:c.1313A>G
|
XP_011537068.1:p.Asp438Gly
|
|
XM_017019980.2:c.2852A>G
|
XP_016875469.1:p.Asp951Gly
|
|
XM_017019981.2:c.2852A>G
|
XP_016875470.1:p.Asp951Gly
|
|
XM_017019982.1:c.2852A>G
|
XP_016875471.1:p.Asp951Gly
|
|
XM_017019983.2:c.1970A>G
|
XP_016875472.1:p.Asp657Gly
|
|
XR_001748869.1:n.3196A>G
|
|
|
XR_001748870.2:n.3196A>G
|
|
|
NM_025114.4:c.1991A>G
MANE Select
|
NP_079390.3:p.Asp664Gly
|
|