ENST00000684241.1:n.3776C=
|
|
|
ENST00000262186.10:c.2943C=
MANE Select
|
ENSP00000262186.5:p.Ser981=
|
|
ENST00000330883.9:c.1923C=
|
ENSP00000328531.4:p.Ser641=
|
|
ENST00000262186.9:c.2943C=
|
ENSP00000262186.5:p.Ser981=
|
|
ENST00000330883.8:c.1923C=
|
ENSP00000328531.4:p.Ser641=
|
|
NM_000238.3:c.2943C= , LRG_288t1:c.2943C=
|
NP_000229.1:p.Ser981=
|
|
NM_172057.2:c.1923C= , LRG_288t3:c.1923C=
|
NP_742054.1:p.Ser641=
|
|
XM_011516185.1:c.2643C=
|
XP_011514487.1:p.Ser881=
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|
XM_011516186.1:c.*23C=
|
XP_011514488.1:n.*23C=
|
|
XM_011516185.2:c.2643C=
|
XP_011514487.1:p.Ser881=
|
|
XM_011516186.3:c.*23C=
|
XP_011514488.1:n.*23C=
|
|
XM_017012195.1:c.2793C=
|
XP_016867684.1:p.Ser931=
|
|
XM_017012196.1:c.2766C=
|
XP_016867685.1:p.Ser922=
|
|
NM_000238.4:c.2943C=
MANE Select
|
NP_000229.1:p.Ser981=
|
|
NM_172057.3:c.1923C=
|
NP_742054.1:p.Ser641=
|
|