ENST00000539215.6:c.147C>G
|
|
|
ENST00000545015.2:n.1466C>G
|
|
|
ENST00000699982.1:c.1293C>G
|
|
|
ENST00000699983.1:c.1293C>G
|
|
|
ENST00000699984.1:c.1293C>G
|
|
|
ENST00000320574.10:c.1439C>G
MANE Select
|
ENSP00000322570.5:p.Ala480Gly
|
|
ENST00000672742.1:c.*941C>G
|
ENSP00000500279.1:n.*941C>G
|
|
ENST00000320574.9:c.1439C>G
|
ENSP00000322570.5:p.Ala480Gly
|
|
ENST00000535270.5:c.1358C>G
|
ENSP00000445753.1:p.Ala453Gly
|
|
ENST00000535934.2:n.1314C>G
|
|
|
ENST00000537064.5:c.*486C>G
|
ENSP00000442578.1:n.*486C>G
|
|
ENST00000539215.5:n.147C>G
|
|
|
ENST00000545015.1:n.36C>G
|
|
|
NM_006231.3:c.1439C>G , LRG_789t1:c.1439C>G
|
NP_006222.2:p.Ala480Gly
|
|
XM_011534795.1:c.1439C>G
|
XP_011533097.1:p.Ala480Gly
|
|
XM_011534796.1:c.1310C>G
|
XP_011533098.1:p.Ala437Gly
|
|
XM_011534797.1:c.518C>G
|
XP_011533099.1:p.Ala173Gly
|
|
XM_011534798.1:c.101C>G
|
XP_011533100.1:p.Ala34Gly
|
|
XM_011534799.1:c.1439C>G
|
XP_011533101.1:p.Ala480Gly
|
|
XM_011534800.1:c.1439C>G
|
XP_011533102.1:p.Ala480Gly
|
|
XM_011534801.1:c.1439C>G
|
XP_011533103.1:p.Ala480Gly
|
|
XR_941395.1:n.1648C>G
|
|
|
XM_011534795.3:c.1439C>G
|
XP_011533097.1:p.Ala480Gly
|
|
XM_011534797.3:c.518C>G
|
XP_011533099.1:p.Ala173Gly
|
|
XM_011534799.2:c.1439C>G
|
XP_011533101.1:p.Ala480Gly
|
|
XR_002957338.1:n.1643C>G
|
|
|
XR_002957339.1:n.1643C>G
|
|
|
XR_941395.2:n.1643C>G
|
|
|
NM_006231.4:c.1439C>G
MANE Select
|
NP_006222.2:p.Ala480Gly
|
|