NM_001558.4:c.301C>A
MANE Select
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NP_001549.2:p.Arg101=
|
ENST00000227752.8:c.301C>A
MANE Select
|
ENSP00000227752.4:p.Arg101=
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NM_001558.3:c.301C>A , LRG_151t1:c.301C>A
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NP_001549.2:p.Arg101=
|
NR_026691.1:n.508C>A
|
|
NR_026691.2:n.505C>A
|
|
ENST00000227752.7:c.301C>A
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ENSP00000227752.3:p.Arg101=
|
ENST00000525467.2:n.649C>A
|
|
ENST00000526544.5:c.188+1052C>A
|
ENSP00000435317.1:n.188+1052C>A
|
ENST00000529924.5:n.1879C>A
|
|
ENST00000529924.6:n.1879C>A
|
|
ENST00000530761.5:n.678C>A
|
|
ENST00000531365.1:n.328C>A
|
|
ENST00000533700.5:n.508C>A
|
|
ENST00000534335.1:n.121C>A
|
|
ENST00000534574.5:c.*241C>A
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ENSP00000436328.1:n.*241C>A
|
ENST00000696732.1:n.2150C>A
|
|
XM_024448493.1:c.-81+1052C>A
|
XP_024304261.1:n.-81+1052C>A
|