ENST00000355832.10:c.3123A>T
MANE Select
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ENSP00000348089.5:p.Gln1041His
|
|
ENST00000679552.1:n.194A>T
|
|
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ENST00000679871.1:n.269A>T
|
|
|
ENST00000679974.1:n.172A>T
|
|
|
ENST00000681632.1:n.4526A>T
|
|
|
ENST00000681659.1:c.2964A>T
|
ENSP00000505631.1:p.Gln988His
|
|
ENST00000355832.9:c.3123A>T
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ENSP00000348089.5:p.Gln1041His
|
|
ENST00000623073.3:c.*1419A>T
|
ENSP00000485650.1:n.*1419A>T
|
|
ENST00000623115.3:c.1233A>T
|
ENSP00000485321.1:p.Gln411His
|
|
ENST00000624341.3:c.955A>T
|
|
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NM_000124.3:c.3123A>T
|
NP_000115.1:p.Gln1041His
|
|
XR_945953.1:n.243-728T>A
|
|
|
NM_001346440.1:c.3123A>T
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NP_001333369.1:p.Gln1041His
|
|
NM_000124.4:c.3123A>T
MANE Select
|
NP_000115.1:p.Gln1041His
|
|
NM_001346440.2:c.3123A>T
|
NP_001333369.1:p.Gln1041His
|
|