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ENST00000644677.1:c.1337A=
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ENSP00000496524.1:p.His446=
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ENST00000644876.2:c.1454A=
MANE Select
|
ENSP00000494040.1:p.His485=
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NM_001193416.2:c.1454A=
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NP_001180345.1:p.His485=
|
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NM_001193417.2:c.1406A=
|
NP_001180346.1:p.His469=
|
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NM_001356.4:c.1454A=
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NP_001347.3:p.His485=
|
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NR_126093.1:n.2399A=
|
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|
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XM_011543892.1:c.1454A=
|
XP_011542194.1:p.His485=
|
|
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NM_001363819.1:c.896A=
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NP_001350748.1:p.His299=
|
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XM_011543892.2:c.1454A=
|
XP_011542194.1:p.His485=
|
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XM_017029313.1:c.896A=
|
XP_016884802.1:p.His299=
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|
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|
|
|
NM_001193417.3:c.1406A=
|
NP_001180346.1:p.His469=
|
|
|
NM_001356.5:c.1454A=
MANE Select
|
NP_001347.3:p.His485=
|
|
