ENST00000242317.9:c.1892G>C
MANE Select
|
ENSP00000242317.4:p.Arg631Thr
|
|
ENST00000242317.8:c.1892G>C
|
ENSP00000242317.4:p.Arg631Thr
|
|
ENST00000442556.1:c.329+2619G>C
|
|
|
ENST00000470169.5:c.680G>C
|
|
|
ENST00000485580.1:n.468G>C
|
|
|
ENST00000614641.4:c.1904G>C
|
ENSP00000480538.1:p.Arg635Thr
|
|
NM_001281428.1:c.1904G>C
|
NP_001268357.1:p.Arg635Thr
|
|
NM_012144.3:c.1892G>C
|
NP_036276.1:p.Arg631Thr
|
|
XM_006716758.2:c.1361G>C
|
XP_006716821.1:p.Arg454Thr
|
|
XM_011517848.1:c.1646G>C
|
XP_011516150.1:p.Arg549Thr
|
|
XM_006716758.3:c.1361G>C
|
XP_006716821.1:p.Arg454Thr
|
|
XM_011517848.2:c.1646G>C
|
XP_011516150.1:p.Arg549Thr
|
|
XM_017014625.2:c.1634G>C
|
XP_016870114.1:p.Arg545Thr
|
|
XR_002956774.1:n.1995G>C
|
|
|
NM_012144.4:c.1892G>C
MANE Select
|
NP_036276.1:p.Arg631Thr
|
|
NM_001281428.2:c.1904G>C
|
NP_001268357.1:p.Arg635Thr
|
|