ENST00000262461.7:c.3604G>A
MANE Select
|
ENSP00000262461.2:p.Gly1202Arg
|
|
ENST00000262461.6:c.3604G>A
|
ENSP00000262461.2:p.Gly1202Arg
|
|
ENST00000343225.4:c.3556G>A
|
ENSP00000340878.4:p.Gly1186Arg
|
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ENST00000509205.5:c.*217G>A
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ENSP00000427109.1:n.*217G>A
|
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NM_001046.2:c.3604G>A
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NP_001037.1:p.Gly1202Arg
|
|
NM_001256461.1:c.3556G>A
|
NP_001243390.1:p.Gly1186Arg
|
|
NR_046207.1:n.3834G>A
|
|
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XM_017009771.1:c.1846G>A
|
XP_016865260.1:p.Gly616Arg
|
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XR_001742214.1:n.3828G>A
|
|
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NM_001046.3:c.3604G>A
MANE Select
|
NP_001037.1:p.Gly1202Arg
|
|
NM_001256461.2:c.3556G>A
|
NP_001243390.1:p.Gly1186Arg
|
|
NR_046207.2:n.3859G>A
|
|
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