ENST00000247933.9:c.785A=
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ENSP00000247933.4:p.His262=
|
|
ENST00000514224.2:c.785A=
MANE Select
|
ENSP00000425081.2:p.His262=
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ENST00000652070.1:n.841A=
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|
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ENST00000247933.8:c.785A=
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ENSP00000247933.4:p.His262=
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ENST00000502910.5:c.644A=
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ENSP00000422952.1:p.His215=
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ENST00000514192.5:c.602A=
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ENSP00000423685.1:p.His201=
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ENST00000514224.1:c.389A=
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ENSP00000425081.1:p.His130=
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ENST00000514698.5:n.685A=
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NM_000203.4:c.785A=
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NP_000194.2:p.His262=
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NR_110313.1:n.873A=
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|
|
XM_006713882.2:c.389A=
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XP_006713945.1:p.His130=
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XM_011513459.1:c.644A=
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XP_011511761.1:p.His215=
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|
XM_011513460.1:c.644A=
|
XP_011511762.1:p.His215=
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|
XM_011513461.1:c.578A=
|
XP_011511763.1:p.His193=
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|
XM_011513462.1:c.497A=
|
XP_011511764.1:p.His166=
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|
XM_011513463.1:c.497A=
|
XP_011511765.1:p.His166=
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|
XR_924947.1:n.854A=
|
|
|
NM_000203.5:c.785A=
MANE Select
|
NP_000194.2:p.His262=
|
|
NM_001363576.1:c.389A=
|
NP_001350505.1:p.His130=
|
|
XM_011513461.2:c.578A=
|
XP_011511763.1:p.His193=
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|
XM_017008163.1:c.-176A=
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XP_016863652.1:n.-176A=
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