ENST00000292408.9:c.575A=
MANE Select
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ENSP00000292408.4:p.His192=
|
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ENST00000292408.8:c.575A=
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ENSP00000292408.4:p.His192=
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ENST00000393637.5:c.575A=
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ENSP00000377254.1:p.His192=
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ENST00000393648.6:c.575A=
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ENSP00000377259.2:p.His192=
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ENST00000426612.5:n.692A=
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ENST00000430285.5:c.*439A=
|
ENSP00000395164.1:n.*439A=
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|
ENST00000502906.5:c.575A=
|
ENSP00000424960.1:p.His192=
|
|
ENST00000503708.5:c.575A=
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ENSP00000424905.1:p.His192=
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|
ENST00000509511.5:n.575A=
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|
|
NM_001291980.1:c.575A=
|
NP_001278909.1:p.His192=
|
|
NM_002011.4:c.575A=
|
NP_002002.3:p.His192=
|
|
NM_022963.3:c.575A=
|
NP_075252.2:p.His192=
|
|
NM_213647.2:c.575A=
|
NP_998812.1:p.His192=
|
|
XM_005265838.2:c.575A=
|
XP_005265895.1:p.His192=
|
|
XM_011534464.1:c.668A=
|
XP_011532766.1:p.His223=
|
|
XM_011534465.1:c.257A=
|
XP_011532767.1:p.His86=
|
|
XR_941090.1:n.620A=
|
|
|
NM_001354984.1:c.575A=
|
NP_001341913.1:p.His192=
|
|
NM_213647.3:c.575A=
MANE Select
|
NP_998812.1:p.His192=
|
|
NM_001291980.2:c.575A=
|
NP_001278909.1:p.His192=
|
|
NM_001354984.2:c.575A=
|
NP_001341913.1:p.His192=
|
|
NM_002011.5:c.575A=
|
NP_002002.3:p.His192=
|
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