ENST00000545015.2:n.43G>C
|
|
|
ENST00000699985.1:n.77G>C
|
|
|
ENST00000320574.10:c.16G>C
MANE Select
|
ENSP00000322570.5:p.Gly6Arg
|
|
ENST00000672742.1:c.16G>C
|
ENSP00000500279.1:p.Gly6Arg
|
|
ENST00000320574.9:c.16G>C
|
ENSP00000322570.5:p.Gly6Arg
|
|
ENST00000535270.5:c.16G>C
|
ENSP00000445753.1:p.Gly6Arg
|
|
ENST00000537064.5:c.16G>C
|
ENSP00000442578.1:p.Gly6Arg
|
|
ENST00000539357.1:n.66G>C
|
|
|
NM_006231.3:c.16G>C , LRG_789t1:c.16G>C
|
NP_006222.2:p.Gly6Arg
|
|
XM_011534795.1:c.16G>C
|
XP_011533097.1:p.Gly6Arg
|
|
XM_011534799.1:c.16G>C
|
XP_011533101.1:p.Gly6Arg
|
|
XM_011534800.1:c.16G>C
|
XP_011533102.1:p.Gly6Arg
|
|
XM_011534801.1:c.16G>C
|
XP_011533103.1:p.Gly6Arg
|
|
XR_941395.1:n.225G>C
|
|
|
XM_011534795.3:c.16G>C
|
XP_011533097.1:p.Gly6Arg
|
|
XM_011534799.2:c.16G>C
|
XP_011533101.1:p.Gly6Arg
|
|
XR_002957338.1:n.220G>C
|
|
|
XR_002957339.1:n.220G>C
|
|
|
XR_941395.2:n.220G>C
|
|
|
NM_006231.4:c.16G>C
MANE Select
|
NP_006222.2:p.Gly6Arg
|
|