ENST00000262367.10:c.6188C=
MANE Select
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ENSP00000262367.5:p.Ser2063=
|
|
ENST00000262367.9:c.6188C=
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ENSP00000262367.5:p.Ser2063=
|
|
ENST00000382070.7:c.6074C=
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ENSP00000371502.3:p.Ser2025=
|
|
NM_001079846.1:c.6074C=
|
NP_001073315.1:p.Ser2025=
|
|
NM_004380.2:c.6188C=
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NP_004371.2:p.Ser2063=
|
|
XM_005255124.3:c.6143C=
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XP_005255181.1:p.Ser2048=
|
|
XM_005255125.3:c.5771C=
|
XP_005255182.1:p.Ser1924=
|
|
XM_006720848.2:c.5927C=
|
XP_006720911.1:p.Ser1976=
|
|
XM_011522380.1:c.6134C=
|
XP_011520682.1:p.Ser2045=
|
|
XM_011522381.1:c.5435C=
|
XP_011520683.1:p.Ser1812=
|
|
XM_005255124.4:c.6143C=
|
XP_005255181.1:p.Ser2048=
|
|
XM_005255125.4:c.5771C=
|
XP_005255182.1:p.Ser1924=
|
|
XM_006720848.3:c.5927C=
|
XP_006720911.1:p.Ser1976=
|
|
XM_011522381.2:c.5435C=
|
XP_011520683.1:p.Ser1812=
|
|
XM_017022944.1:c.6182C=
|
XP_016878433.1:p.Ser2061=
|
|
NM_004380.3:c.6188C=
MANE Select
|
NP_004371.2:p.Ser2063=
|
|