ENST00000383408.7:c.5675G>T
|
ENSP00000372900.4:p.Gly1892Val
|
|
ENST00000643712.1:c.683G>T
|
ENSP00000493635.1:p.Gly228Val
|
|
ENST00000674853.1:c.5939G>T
MANE Select
|
ENSP00000501957.1:p.Gly1980Val
|
|
ENST00000302079.10:c.5600G>T
|
ENSP00000303316.6:p.Gly1867Val
|
|
ENST00000383408.6:c.5453G>T
|
ENSP00000372900.3:p.Gly1818Val
|
|
ENST00000503781.7:c.5600G>T
|
ENSP00000421377.3:p.Gly1867Val
|
|
ENST00000580640.5:c.5675G>T
|
ENSP00000463094.1:p.Gly1892Val
|
|
ENST00000582913.5:c.5806G>T
|
ENSP00000462115.1:n.5806G>T
|
|
NM_022068.3:c.5600G>T
|
NP_071351.2:p.Gly1867Val
|
|
XM_011525723.1:c.5732G>T
|
XP_011524025.1:p.Gly1911Val
|
|
XM_011525724.1:c.5675G>T
|
XP_011524026.1:p.Gly1892Val
|
|
XM_011525725.1:c.5642G>T
|
XP_011524027.1:p.Gly1881Val
|
|
XM_011525726.1:c.5732G>T
|
XP_011524028.1:p.Gly1911Val
|
|
XM_011525723.3:c.5732G>T
|
XP_011524025.1:p.Gly1911Val
|
|
XM_011525724.3:c.5675G>T
|
XP_011524026.1:p.Gly1892Val
|
|
XM_011525725.3:c.5642G>T
|
XP_011524027.1:p.Gly1881Val
|
|
XM_011525726.3:c.5732G>T
|
XP_011524028.1:p.Gly1911Val
|
|
XM_017025918.2:c.5693G>T
|
XP_016881407.1:p.Gly1898Val
|
|
XR_001753259.2:n.6729G>T
|
|
|
NM_001378183.1:c.5939G>T
MANE Select
|
NP_001365112.1:p.Gly1980Val
|
|
NM_022068.4:c.5600G>T
|
NP_071351.2:p.Gly1867Val
|
|