ENST00000350026.11:c.3068C>G
|
ENSP00000055163.8:p.Ala1023Gly
|
|
ENST00000414678.8:c.2978C>G
|
ENSP00000412835.3:p.Ala993Gly
|
|
ENST00000637015.2:c.3068C>G
|
ENSP00000489729.2:p.Ala1023Gly
|
|
ENST00000319584.11:c.1082C>G
|
ENSP00000313006.7:p.Ala361Gly
|
|
ENST00000346085.10:c.3107C>G
|
ENSP00000344546.5:p.Ala1036Gly
|
|
ENST00000350026.10:c.2819C>G
|
ENSP00000055163.7:p.Ala940Gly
|
|
ENST00000414678.7:c.1226C>G
|
ENSP00000412835.2:p.Ala409Gly
|
|
ENST00000452544.2:n.969C>G
|
|
|
ENST00000635849.1:c.389C>G
|
ENSP00000490948.1:p.Ala130Gly
|
|
ENST00000635957.1:c.23C>G
|
ENSP00000490385.1:p.Ala8Gly
|
|
ENST00000636426.1:n.202C>G
|
|
|
ENST00000636930.2:c.3068C>G
MANE Select
|
ENSP00000490491.2:p.Ala1023Gly
|
|
ENST00000637015.1:c.307C>G
|
|
|
ENST00000637568.1:c.111C>G
|
|
|
ENST00000637810.1:c.569C>G
|
ENSP00000489636.1:p.Ala190Gly
|
|
ENST00000637904.1:c.569C>G
|
ENSP00000490550.1:p.Ala190Gly
|
|
ENST00000647938.1:c.2858C>G
|
ENSP00000498155.1:p.Ala953Gly
|
|
ENST00000674190.1:n.1817C>G
|
|
|
ENST00000319584.10:c.1085C>G
|
ENSP00000313006.6:p.Ala362Gly
|
|
ENST00000346085.9:c.2858C>G
|
ENSP00000344546.4:p.Ala953Gly
|
|
ENST00000350026.9:c.2819C>G
|
ENSP00000055163.7:p.Ala940Gly
|
|
ENST00000400790.3:c.20C>G
|
ENSP00000383596.3:p.Ala7Gly
|
|
ENST00000414678.6:c.1226C>G
|
ENSP00000412835.2:p.Ala409Gly
|
|
ENST00000452544.1:n.915C>G
|
|
|
ENST00000478761.3:c.141C>G
|
|
|
NM_017519.2:c.2819C>G
|
NP_059989.2:p.Ala940Gly
|
|
NM_020732.3:c.2858C>G
|
NP_065783.3:p.Ala953Gly
|
|
XM_005267069.3:c.2819C>G
|
XP_005267126.2:p.Ala940Gly
|
|
XM_011535984.1:c.1769C>G
|
XP_011534286.1:p.Ala590Gly
|
|
XM_011535985.1:c.1589C>G
|
XP_011534287.1:p.Ala530Gly
|
|
XM_011535986.1:c.1349C>G
|
XP_011534288.1:p.Ala450Gly
|
|
XM_011535987.1:c.968C>G
|
XP_011534289.1:p.Ala323Gly
|
|
XM_011535988.1:c.-20+15723C>G
|
XP_011534290.1:n.-20+15723C>G
|
|
NM_001346813.1:c.2819C>G
|
NP_001333742.1:p.Ala940Gly
|
|
NM_001363725.1:c.569C>G
|
NP_001350654.1:p.Ala190Gly
|
|
XM_011535984.2:c.2900C>G
|
XP_011534286.2:p.Ala967Gly
|
|
XM_011535988.3:c.-20+15723C>G
|
XP_011534290.1:n.-20+15723C>G
|
|
XM_017011103.2:c.2900C>G
|
XP_016866592.1:p.Ala967Gly
|
|
XM_017011104.1:c.2900C>G
|
XP_016866593.1:p.Ala967Gly
|
|
XM_017011105.2:c.2900C>G
|
XP_016866594.1:p.Ala967Gly
|
|
XM_017011106.2:c.2900C>G
|
XP_016866595.1:p.Ala967Gly
|
|
XM_017011107.2:c.2720C>G
|
XP_016866596.1:p.Ala907Gly
|
|
XR_002956289.1:n.2983C>G
|
|
|
NM_001363725.2:c.569C>G
|
NP_001350654.1:p.Ala190Gly
|
|
NM_001371656.1:c.3107C>G
|
NP_001358585.1:p.Ala1036Gly
|
|
NM_001374820.1:c.3107C>G
|
NP_001361749.1:p.Ala1036Gly
|
|
NM_001374828.1:c.3068C>G
MANE Select
|
NP_001361757.1:p.Ala1023Gly
|
|
NM_017519.3:c.3068C>G
|
NP_059989.3:p.Ala1023Gly
|
|