NM_000170.3:c.2258A=
MANE Select
|
NP_000161.2:p.His753=
|
ENST00000321612.8:c.2258A=
MANE Select
|
ENSP00000370737.4:p.His753=
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NM_000170.2:c.2258A= , LRG_643t1:c.2258A=
|
NP_000161.2:p.His753=
|
ENST00000321612.6:c.2258A=
|
ENSP00000370737.3:p.His753=
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ENST00000467946.1:n.184A=
|
|
ENST00000638233.1:n.693A=
|
|
ENST00000638661.1:c.458A=
|
ENSP00000491369.1:p.His153=
|
ENST00000638694.1:n.445A=
|
|
ENST00000639318.1:c.458A=
|
ENSP00000491932.1:p.His153=
|
ENST00000639364.1:n.1958A=
|
|
ENST00000639443.1:n.1826A=
|
|
ENST00000639639.1:c.-41A=
|
ENSP00000491312.1:n.-41A=
|
ENST00000639954.1:n.1966A=
|
|
ENST00000640505.1:n.497A=
|
|