ENST00000301305.8:c.280G=
MANE Select
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ENSP00000301305.4:p.Ala94=
|
|
ENST00000276833.9:c.205G=
|
ENSP00000276833.5:p.Ala69=
|
|
ENST00000301305.7:c.280G=
|
ENSP00000301305.3:p.Ala94=
|
|
ENST00000526658.1:c.193-585G=
|
ENSP00000434512.1:n.193-585G=
|
|
NM_017767.2:c.205G=
|
NP_060237.2:p.Ala69=
|
|
NM_130849.3:c.280G=
|
NP_570901.2:p.Ala94=
|
|
XM_006716599.1:c.280G=
|
XP_006716662.1:p.Ala94=
|
|
XM_011517153.1:c.193-585G=
|
XP_011515455.1:n.193-585G=
|
|
XM_024447188.1:c.193-585G=
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XP_024302956.1:n.193-585G=
|
|
XM_024447189.1:c.193-585G=
|
XP_024302957.1:n.193-585G=
|
|
NM_001374839.1:c.193-585G=
|
NP_001361768.1:n.193-585G=
|
|
NM_017767.3:c.205G=
|
NP_060237.3:p.Ala69=
|
|
NM_130849.4:c.280G=
MANE Select
|
NP_570901.3:p.Ala94=
|
|