ENST00000342245.9:c.1710G>C
MANE Select
|
ENSP00000340409.4:p.Gln570His
|
|
ENST00000342245.8:c.1710G>C
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ENSP00000340409.4:p.Gln570His
|
|
ENST00000526280.1:c.767G>C
|
|
|
ENST00000527275.5:c.1707G>C
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ENSP00000435350.1:p.Gln569His
|
|
ENST00000531303.5:c.*561G>C
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ENSP00000432625.1:n.*561G>C
|
|
ENST00000533123.5:c.*437G>C
|
ENSP00000435950.1:n.*437G>C
|
|
ENST00000534405.5:c.*541G>C
|
ENSP00000434353.1:n.*541G>C
|
|
NM_000543.4:c.1710G>C
|
NP_000534.3:p.Gln570His
|
|
NM_001007593.2:c.1707G>C
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NP_001007594.2:p.Gln569His
|
|
XM_005253075.3:c.*203G>C
|
XP_005253132.1:n.*203G>C
|
|
XM_011520303.1:c.1578G>C
|
XP_011518605.1:p.Gln526His
|
|
XM_011520304.1:c.*203G>C
|
XP_011518606.1:n.*203G>C
|
|
NM_001318087.1:c.*203G>C
|
NP_001305016.1:n.*203G>C
|
|
NM_001318088.1:c.789G>C
|
NP_001305017.1:p.Gln263His
|
|
NM_001365135.1:c.1578G>C
|
NP_001352064.1:p.Gln526His
|
|
NR_027400.2:n.1723G>C
|
|
|
NR_134502.1:n.1262G>C
|
|
|
XM_011520304.2:c.*203G>C
|
XP_011518606.1:n.*203G>C
|
|
XR_001747940.2:n.1895G>C
|
|
|
XR_002957158.1:n.2077G>C
|
|
|
NM_000543.5:c.1710G>C
MANE Select
|
NP_000534.3:p.Gln570His
|
|
NM_001007593.3:c.1707G>C
|
NP_001007594.2:p.Gln569His
|
|
NM_001318087.2:c.*203G>C
|
NP_001305016.1:n.*203G>C
|
|
NM_001318088.2:c.789G>C
|
NP_001305017.1:p.Gln263His
|
|
NM_001365135.2:c.1578G>C
|
NP_001352064.1:p.Gln526His
|
|
NR_027400.3:n.1663G>C
|
|
|
NR_134502.2:n.1202G>C
|
|
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