ENST00000295897.9:c.474T=
MANE Select
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ENSP00000295897.4:p.Phe158=
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ENST00000295897.8:c.474T=
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ENSP00000295897.4:p.Phe158=
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ENST00000401494.7:c.138-558T=
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ENSP00000384695.3:n.138-558T=
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ENST00000415165.6:c.138-3199T=
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ENSP00000401820.2:n.138-3199T=
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ENST00000441319.5:c.480T=
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ENSP00000392541.1:p.Phe160=
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|
ENST00000476441.6:c.80-558T=
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ENSP00000423727.1:n.80-558T=
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ENST00000503124.5:c.33-558T=
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ENSP00000421027.1:n.33-558T=
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ENST00000505649.5:n.160T=
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|
|
ENST00000509063.5:c.474T=
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ENSP00000422784.1:p.Phe158=
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|
ENST00000510166.5:n.510T=
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|
|
ENST00000514786.1:n.443T=
|
|
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ENST00000515133.5:n.515T=
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|
|
ENST00000621085.4:c.474T=
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ENSP00000483421.1:p.Phe158=
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|
ENST00000621628.4:c.474T=
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ENSP00000480485.1:p.Phe158=
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|
NM_000477.5:c.474T=
|
NP_000468.1:p.Phe158=
|
|
NM_000477.6:c.474T=
|
NP_000468.1:p.Phe158=
|
|
NM_000477.7:c.474T=
MANE Select
|
NP_000468.1:p.Phe158=
|
|