ENST00000248633.9:c.2346A>C
MANE Select
|
ENSP00000248633.4:p.Arg782Ser
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|
ENST00000248633.8:c.2346A>C
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ENSP00000248633.4:p.Arg782Ser
|
|
ENST00000428214.5:c.2175A>C
|
ENSP00000394413.1:p.Arg725Ser
|
|
ENST00000438045.5:c.1380A>C
|
ENSP00000410438.1:p.Arg460Ser
|
|
ENST00000484913.5:n.2385A>C
|
|
|
ENST00000496092.1:n.144A>C
|
|
|
ENST00000496420.5:n.2022A>C
|
|
|
NM_000466.2:c.2346A>C
|
NP_000457.1:p.Arg782Ser
|
|
NM_001282677.1:c.2175A>C
|
NP_001269606.1:p.Arg725Ser
|
|
NM_001282678.1:c.1722A>C
|
NP_001269607.1:p.Arg574Ser
|
|
XM_005250433.3:c.597A>C
|
XP_005250490.1:p.Arg199Ser
|
|
XR_242246.3:n.2442A>C
|
|
|
XM_017012319.2:c.597A>C
|
XP_016867808.1:p.Arg199Ser
|
|
XR_001744808.2:n.1373A>C
|
|
|
XR_242246.5:n.2393A>C
|
|
|
NM_000466.3:c.2346A>C
MANE Select
|
NP_000457.1:p.Arg782Ser
|
|
NM_001282677.2:c.2175A>C
|
NP_001269606.1:p.Arg725Ser
|
|
NM_001282678.2:c.1722A>C
|
NP_001269607.1:p.Arg574Ser
|
|