ENST00000317961.9:c.3591T>A
MANE Select
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ENSP00000322408.4:p.His1197Gln
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|
ENST00000317961.8:c.3591T>A
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ENSP00000322408.4:p.His1197Gln
|
|
ENST00000382806.6:c.3420T>A
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ENSP00000372256.2:p.His1140Gln
|
|
ENST00000415360.1:c.507T>A
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ENSP00000389433.1:p.His169Gln
|
|
ENST00000440077.5:c.3468T>A
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ENSP00000398543.1:p.His1156Gln
|
|
ENST00000469599.6:n.2189T>A
|
|
|
ENST00000492117.1:n.3483T>A
|
|
|
ENST00000541639.5:c.3684T>A
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ENSP00000444293.1:p.His1228Gln
|
|
NM_001146705.1:c.3684T>A
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NP_001140177.1:p.His1228Gln
|
|
NM_001146706.1:c.3420T>A
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NP_001140178.1:p.His1140Gln
|
|
NM_004653.4:c.3591T>A
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NP_004644.2:p.His1197Gln
|
|
XM_005262560.1:c.3456T>A
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XP_005262617.1:p.His1152Gln
|
|
XM_005262561.1:c.3360T>A
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XP_005262618.1:p.His1120Gln
|
|
XM_011531468.1:c.3513T>A
|
XP_011529770.1:p.His1171Gln
|
|
XR_244571.2:n.3879T>A
|
|
|
XR_430568.2:n.4213T>A
|
|
|
XM_005262560.3:c.3456T>A
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XP_005262617.1:p.His1152Gln
|
|
XM_005262561.3:c.3360T>A
|
XP_005262618.1:p.His1120Gln
|
|
XM_011531468.3:c.3513T>A
|
XP_011529770.1:p.His1171Gln
|
|
XM_024452495.1:c.1581T>A
|
XP_024308263.1:p.His527Gln
|
|
XM_024452496.1:c.1347T>A
|
XP_024308264.1:p.His449Gln
|
|
XR_001756009.2:n.4329T>A
|
|
|
XR_001756010.2:n.4329T>A
|
|
|
XR_001756011.2:n.4194T>A
|
|
|
XR_001756012.2:n.4342T>A
|
|
|
XR_001756013.2:n.3660T>A
|
|
|
XR_002958832.1:n.3761T>A
|
|
|
XR_002958834.1:n.3985T>A
|
|
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XR_002958835.1:n.3868T>A
|
|
|
XR_002958836.1:n.4551T>A
|
|
|
XR_002958837.1:n.4358T>A
|
|
|
XR_244571.4:n.3878T>A
|
|
|
XR_430568.4:n.4212T>A
|
|
|
NM_001146706.2:c.3420T>A
|
NP_001140178.1:p.His1140Gln
|
|
NM_004653.5:c.3591T>A
MANE Select
|
NP_004644.2:p.His1197Gln
|
|
NM_001146705.2:c.3684T>A
|
NP_001140177.1:p.His1228Gln
|
|