ENST00000281928.9:c.5008A>C
MANE Select
|
ENSP00000281928.3:p.Ser1670Arg
|
|
ENST00000549786.2:c.4436A>C
|
|
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ENST00000648379.1:n.3376A>C
|
|
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ENST00000648737.1:n.4772A>C
|
|
|
ENST00000648825.1:n.1748A>C
|
|
|
ENST00000648916.1:n.3019A>C
|
|
|
ENST00000649146.1:n.2251A>C
|
|
|
ENST00000649607.1:c.3192A>C
|
|
|
ENST00000649775.1:c.1497A>C
|
|
|
ENST00000650226.1:c.5008A>C
|
ENSP00000496981.1:p.Ser1670Arg
|
|
ENST00000281928.7:c.5008A>C
|
ENSP00000281928.3:p.Ser1670Arg
|
|
ENST00000549786.1:c.372A>C
|
|
|
ENST00000552340.1:c.40A>C
|
ENSP00000449876.1:p.Ser14Arg
|
|
NM_015335.4:c.5008A>C
|
NP_056150.1:p.Ser1670Arg
|
|
XM_011538080.1:c.5008A>C
|
XP_011536382.1:p.Ser1670Arg
|
|
XM_011538081.1:c.5005A>C
|
XP_011536383.1:p.Ser1669Arg
|
|
XM_011538082.1:c.4978A>C
|
XP_011536384.1:p.Ser1660Arg
|
|
XM_011538080.2:c.5008A>C
|
XP_011536382.1:p.Ser1670Arg
|
|
XM_011538081.2:c.5005A>C
|
XP_011536383.1:p.Ser1669Arg
|
|
XM_011538082.2:c.4978A>C
|
XP_011536384.1:p.Ser1660Arg
|
|
XM_017019090.1:c.5005A>C
|
XP_016874579.1:p.Ser1669Arg
|
|
NM_015335.5:c.5008A>C
MANE Select
|
NP_056150.1:p.Ser1670Arg
|
|