ENST00000559133.6:c.6156G>C
|
ENSP00000453958.2:p.Arg2052Ser
|
|
ENST00000674301.2:c.6156G>C
|
ENSP00000501333.2:p.Arg2052Ser
|
|
ENST00000316623.10:c.6156G>C
MANE Select
|
ENSP00000325527.5:p.Arg2052Ser
|
|
ENST00000674301.1:c.1155G>C
|
ENSP00000501333.1:p.Arg385Ser
|
|
ENST00000316623.9:c.6156G>C
|
ENSP00000325527.5:p.Arg2052Ser
|
|
ENST00000537463.6:c.*1919G>C
|
ENSP00000440294.2:n.*1919G>C
|
|
ENST00000559133.5:c.1463G>C
|
|
|
ENST00000560820.1:n.276G>C
|
|
|
NM_000138.4:c.6156G>C , LRG_778t1:c.6156G>C
|
NP_000129.3:p.Arg2052Ser
|
|
NM_000138.5:c.6156G>C
MANE Select
|
NP_000129.3:p.Arg2052Ser
|
|