ENST00000394867.9:n.1629G>C
|
|
|
ENST00000688002.1:n.3341G>C
|
|
|
ENST00000688751.1:n.326G>C
|
|
|
ENST00000689792.1:n.1094G>C
|
|
|
ENST00000262948.10:c.1190G>C
MANE Select
|
ENSP00000262948.4:p.Arg397Pro
|
|
ENST00000262948.9:c.1190G>C
|
ENSP00000262948.3:p.Arg397Pro
|
|
ENST00000394867.8:c.899G>C
|
ENSP00000378336.1:p.Arg300Pro
|
|
ENST00000597263.5:n.375G>C
|
|
|
ENST00000599021.1:c.300G>C
|
|
|
ENST00000600584.5:n.2639G>C
|
|
|
ENST00000601786.5:n.1491G>C
|
|
|
NM_030662.3:c.1190G>C , LRG_750t1:c.1190G>C
|
NP_109587.1:p.Arg397Pro
|
|
XM_006722799.2:c.911G>C
|
XP_006722862.1:p.Arg304Pro
|
|
XM_011528133.1:c.620G>C
|
XP_011526435.1:p.Arg207Pro
|
|
NM_030662.4:c.1190G>C
MANE Select
|
NP_109587.1:p.Arg397Pro
|
|