ENST00000542664.4:c.447A=
MANE Select
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ENSP00000437737.1:p.Ala149=
|
|
ENST00000543956.5:c.-43A=
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ENSP00000441861.2:n.-43A=
|
|
ENST00000378688.8:c.447A=
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ENSP00000367959.3:p.Ala149=
|
|
ENST00000542664.3:c.447A=
|
ENSP00000437737.1:p.Ala149=
|
|
ENST00000543956.4:c.195A=
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ENSP00000441861.1:p.Ala65=
|
|
NM_000621.4:c.447A=
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NP_000612.1:p.Ala149=
|
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NM_001165947.2:c.195A=
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NP_001159419.1:p.Ala65=
|
|
NM_000621.5:c.447A=
MANE Select
|
NP_000612.1:p.Ala149=
|
|
NM_001165947.5:c.-43A=
|
NP_001159419.2:n.-43A=
|
|
NM_001378924.1:c.447A=
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NP_001365853.1:p.Ala149=
|
|