ENST00000248633.9:c.2635T=
MANE Select
|
ENSP00000248633.4:p.Leu879=
|
|
ENST00000248633.8:c.2635T=
|
ENSP00000248633.4:p.Leu879=
|
|
ENST00000428214.5:c.2464T=
|
ENSP00000394413.1:p.Leu822=
|
|
ENST00000438045.5:c.1669T=
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ENSP00000410438.1:p.Leu557=
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|
ENST00000484913.5:n.2674T=
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|
|
ENST00000496420.5:n.2527T=
|
|
|
NM_000466.2:c.2635T=
|
NP_000457.1:p.Leu879=
|
|
NM_001282677.1:c.2464T=
|
NP_001269606.1:p.Leu822=
|
|
NM_001282678.1:c.2011T=
|
NP_001269607.1:p.Leu671=
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|
XM_005250433.3:c.886T=
|
XP_005250490.1:p.Leu296=
|
|
XR_242246.3:n.2731T=
|
|
|
XM_017012319.2:c.886T=
|
XP_016867808.1:p.Leu296=
|
|
XR_001744808.2:n.1662T=
|
|
|
XR_242246.5:n.2682T=
|
|
|
NM_000466.3:c.2635T=
MANE Select
|
NP_000457.1:p.Leu879=
|
|
NM_001282677.2:c.2464T=
|
NP_001269606.1:p.Leu822=
|
|
NM_001282678.2:c.2011T=
|
NP_001269607.1:p.Leu671=
|
|