ENST00000355832.10:c.3616C>G
MANE Select
|
ENSP00000348089.5:p.Pro1206Ala
|
|
ENST00000679552.1:n.687C>G
|
|
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ENST00000679871.1:n.762C>G
|
|
|
ENST00000679974.1:n.665C>G
|
|
|
ENST00000681632.1:n.5019C>G
|
|
|
ENST00000681659.1:c.3457C>G
|
ENSP00000505631.1:p.Pro1153Ala
|
|
ENST00000355832.9:c.3616C>G
|
ENSP00000348089.5:p.Pro1206Ala
|
|
ENST00000623073.3:c.*1912C>G
|
ENSP00000485650.1:n.*1912C>G
|
|
ENST00000623115.3:c.1726C>G
|
ENSP00000485321.1:p.Pro576Ala
|
|
ENST00000624341.3:c.1448C>G
|
|
|
NM_000124.3:c.3616C>G
|
NP_000115.1:p.Pro1206Ala
|
|
XR_945953.1:n.243-1221G>C
|
|
|
NM_001346440.1:c.3616C>G
|
NP_001333369.1:p.Pro1206Ala
|
|
NM_000124.4:c.3616C>G
MANE Select
|
NP_000115.1:p.Pro1206Ala
|
|
NM_001346440.2:c.3616C>G
|
NP_001333369.1:p.Pro1206Ala
|
|