ENST00000355832.10:c.2937G>A
MANE Select
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ENSP00000348089.5:p.Lys979=
|
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ENST00000679552.1:n.142-219G>A
|
|
|
ENST00000679871.1:n.83G>A
|
|
|
ENST00000679974.1:n.120-219G>A
|
|
|
ENST00000681632.1:n.4340G>A
|
|
|
ENST00000681659.1:c.2778G>A
|
ENSP00000505631.1:p.Lys926=
|
|
ENST00000355832.9:c.2937G>A
|
ENSP00000348089.5:p.Lys979=
|
|
ENST00000623073.3:c.*1233G>A
|
ENSP00000485650.1:n.*1233G>A
|
|
ENST00000623115.3:c.1047G>A
|
ENSP00000485321.1:p.Lys349=
|
|
ENST00000624341.3:c.769G>A
|
|
|
NM_000124.3:c.2937G>A
|
NP_000115.1:p.Lys979=
|
|
XR_945953.1:n.243-457C>T
|
|
|
NM_001346440.1:c.2937G>A
|
NP_001333369.1:p.Lys979=
|
|
NM_000124.4:c.2937G>A
MANE Select
|
NP_000115.1:p.Lys979=
|
|
NM_001346440.2:c.2937G>A
|
NP_001333369.1:p.Lys979=
|
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