ENST00000355832.10:c.3272T>G
MANE Select
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ENSP00000348089.5:p.Leu1091Trp
|
|
ENST00000679552.1:n.343T>G
|
|
|
ENST00000679871.1:n.418T>G
|
|
|
ENST00000679974.1:n.321T>G
|
|
|
ENST00000681632.1:n.4675T>G
|
|
|
ENST00000681659.1:c.3113T>G
|
ENSP00000505631.1:p.Leu1038Trp
|
|
ENST00000355832.9:c.3272T>G
|
ENSP00000348089.5:p.Leu1091Trp
|
|
ENST00000623073.3:c.*1568T>G
|
ENSP00000485650.1:n.*1568T>G
|
|
ENST00000623115.3:c.1382T>G
|
ENSP00000485321.1:p.Leu461Trp
|
|
ENST00000624341.3:c.1104T>G
|
|
|
NM_000124.3:c.3272T>G
|
NP_000115.1:p.Leu1091Trp
|
|
XR_945953.1:n.243-877A>C
|
|
|
NM_001346440.1:c.3272T>G
|
NP_001333369.1:p.Leu1091Trp
|
|
NM_000124.4:c.3272T>G
MANE Select
|
NP_000115.1:p.Leu1091Trp
|
|
NM_001346440.2:c.3272T>G
|
NP_001333369.1:p.Leu1091Trp
|
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