ENST00000339818.9:c.267G=
MANE Select
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ENSP00000344566.4:p.Leu89=
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ENST00000325223.7:c.267G=
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ENSP00000317302.7:p.Leu89=
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ENST00000339818.8:c.267G=
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ENSP00000344566.4:p.Leu89=
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ENST00000397956.7:c.267G=
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ENSP00000381047.3:p.Leu89=
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ENST00000462742.1:n.2438G=
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ENST00000478674.1:n.326G=
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ENST00000496321.5:n.383G=
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NM_001271440.1:c.267G=
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NP_001258369.1:p.Leu89=
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NM_001271441.1:c.267G=
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NP_001258370.1:p.Leu89=
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NM_001271442.1:c.144G=
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NP_001258371.1:p.Leu48=
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NM_004928.2:c.267G=
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NP_004919.1:p.Leu89=
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XM_006724051.2:c.342G=
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XP_006724114.1:p.Leu114=
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XM_006724052.2:c.342G=
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XP_006724115.1:p.Leu114=
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XM_006724053.2:c.-58G=
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XP_006724116.1:n.-58G=
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XR_937571.1:n.470G=
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XM_006724051.3:c.342G=
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XP_006724114.1:p.Leu114=
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XM_006724053.3:c.-58G=
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XP_006724116.1:n.-58G=
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XM_017028470.1:c.471G=
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XP_016883959.1:p.Leu157=
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XM_017028471.1:c.216G=
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XP_016883960.1:p.Leu72=
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XM_017028472.1:c.-58G=
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XP_016883961.1:n.-58G=
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XR_937571.2:n.477G=
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NM_004928.3:c.267G=
MANE Select
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NP_004919.1:p.Leu89=
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NM_001271440.2:c.267G=
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NP_001258369.1:p.Leu89=
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NM_001271441.2:c.267G=
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NP_001258370.1:p.Leu89=
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