ENST00000264595.7:c.381A>G
MANE Select
|
ENSP00000264595.2:p.Leu127=
|
|
ENST00000264595.6:c.381A>G
|
ENSP00000264595.2:p.Leu127=
|
|
ENST00000502310.5:c.36A>G
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ENSP00000423798.1:p.Leu12=
|
|
ENST00000506853.5:n.415A>G
|
|
|
ENST00000510635.1:c.77A>G
|
|
|
ENST00000510955.5:n.315+684A>G
|
|
|
NM_000027.3:c.381A>G
|
NP_000018.2:p.Leu127=
|
|
NM_001171988.1:c.381A>G
|
NP_001165459.1:p.Leu127=
|
|
NR_033655.1:n.509A>G
|
|
|
XM_006714123.2:c.381A>G
|
XP_006714186.1:p.Leu127=
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XR_001741155.2:n.475A>G
|
|
|
NM_000027.4:c.381A>G
MANE Select
|
NP_000018.2:p.Leu127=
|
|
NM_001171988.2:c.381A>G
|
NP_001165459.1:p.Leu127=
|
|
NR_033655.2:n.443A>G
|
|
|