ENST00000636937.2:c.1828T=
|
ENSP00000516154.1:p.Phe610=
|
|
ENST00000268124.11:c.1828T=
MANE Select
|
ENSP00000268124.5:p.Phe610=
|
|
ENST00000530292.3:c.1429T=
|
ENSP00000432885.2:p.Phe477=
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|
ENST00000635986.2:c.1828T=
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ENSP00000490653.2:p.Phe610=
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|
ENST00000636774.1:c.*395T=
|
ENSP00000489799.1:n.*395T=
|
|
ENST00000637238.1:c.565T=
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ENSP00000490756.1:p.Phe189=
|
|
ENST00000637264.1:c.900T=
|
|
|
ENST00000666746.1:c.1405T=
|
|
|
ENST00000670281.1:c.148T=
|
ENSP00000499709.1:p.Phe50=
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|
ENST00000672071.1:n.2026T=
|
|
|
ENST00000672923.2:n.1931T=
|
|
|
ENST00000268124.9:c.1828T=
|
ENSP00000268124.5:p.Phe610=
|
|
ENST00000442287.6:c.1828T=
|
ENSP00000399851.2:p.Phe610=
|
|
ENST00000526314.2:c.210T=
|
|
|
ENST00000526398.1:c.17T=
|
|
|
ENST00000532584.5:n.30T=
|
|
|
ENST00000631044.2:c.*1211T=
|
ENSP00000486730.1:n.*1211T=
|
|
NM_001126131.1:c.1828T=
|
NP_001119603.1:p.Phe610=
|
|
NM_002693.2:c.1828T=
|
NP_002684.1:p.Phe610=
|
|
NM_001126131.2:c.1828T=
|
NP_001119603.1:p.Phe610=
|
|
NM_002693.3:c.1828T=
MANE Select
|
NP_002684.1:p.Phe610=
|
|