ENST00000684241.1:n.3763G>C
|
|
|
ENST00000262186.10:c.2930G>C
MANE Select
|
ENSP00000262186.5:p.Cys977Ser
|
|
ENST00000330883.9:c.1910G>C
|
ENSP00000328531.4:p.Cys637Ser
|
|
ENST00000262186.9:c.2930G>C
|
ENSP00000262186.5:p.Cys977Ser
|
|
ENST00000330883.8:c.1910G>C
|
ENSP00000328531.4:p.Cys637Ser
|
|
NM_000238.3:c.2930G>C , LRG_288t1:c.2930G>C
|
NP_000229.1:p.Cys977Ser
|
|
NM_172057.2:c.1910G>C , LRG_288t3:c.1910G>C
|
NP_742054.1:p.Cys637Ser
|
|
XM_011516185.1:c.2630G>C
|
XP_011514487.1:p.Cys877Ser
|
|
XM_011516186.1:c.*10G>C
|
XP_011514488.1:n.*10G>C
|
|
XM_011516185.2:c.2630G>C
|
XP_011514487.1:p.Cys877Ser
|
|
XM_011516186.3:c.*10G>C
|
XP_011514488.1:n.*10G>C
|
|
XM_017012195.1:c.2780G>C
|
XP_016867684.1:p.Cys927Ser
|
|
XM_017012196.1:c.2753G>C
|
XP_016867685.1:p.Cys918Ser
|
|
NM_000238.4:c.2930G>C
MANE Select
|
NP_000229.1:p.Cys977Ser
|
|
NM_172057.3:c.1910G>C
|
NP_742054.1:p.Cys637Ser
|
|