ENST00000348931.9:c.569A=
MANE Select
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ENSP00000335384.5:p.His190=
|
|
ENST00000348931.8:c.569A=
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ENSP00000335384.5:p.His190=
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|
ENST00000377940.3:c.503A=
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ENSP00000367174.3:p.His168=
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|
ENST00000583811.5:c.215A=
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ENSP00000462463.1:p.His72=
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|
ENST00000584588.5:c.407-612A=
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ENSP00000462067.1:n.407-612A=
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|
NM_198844.2:c.503A=
|
NP_942141.2:p.His168=
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|
NM_199321.2:c.569A=
|
NP_955353.1:p.His190=
|
|
XM_011524298.1:c.569A=
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XP_011522600.1:p.His190=
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|
XR_002957959.1:n.760A=
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|
|
NM_198844.3:c.503A=
|
NP_942141.2:p.His168=
|
|
NM_199321.3:c.569A=
MANE Select
|
NP_955353.1:p.His190=
|
|