ENST00000303941.4:c.2047G=
MANE Select
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ENSP00000306678.3:p.Ala683=
|
|
ENST00000303941.3:c.2047G=
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ENSP00000306678.3:p.Ala683=
|
|
NM_178510.1:c.2047G=
|
NP_848605.1:p.Ala683=
|
|
XM_011542736.1:c.2080G=
|
XP_011541038.1:p.Ala694=
|
|
XM_011542737.1:c.2050G=
|
XP_011541039.1:p.Ala684=
|
|
XM_011542738.1:c.1858G=
|
XP_011541040.1:p.Ala620=
|
|
XM_011542736.2:c.2080G=
|
XP_011541038.1:p.Ala694=
|
|
XM_011542737.2:c.2050G=
|
XP_011541039.1:p.Ala684=
|
|
XM_011542738.2:c.1858G=
|
XP_011541040.1:p.Ala620=
|
|
XM_017017475.1:c.2077G=
|
XP_016872964.1:p.Ala693=
|
|
NM_178510.2:c.2047G=
MANE Select
|
NP_848605.1:p.Ala683=
|
|