ENST00000355832.10:c.3980A>C
MANE Select
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ENSP00000348089.5:p.Lys1327Thr
|
|
ENST00000679552.1:n.1051A>C
|
|
|
ENST00000679871.1:n.1126A>C
|
|
|
ENST00000679974.1:n.1029A>C
|
|
|
ENST00000681632.1:n.5383A>C
|
|
|
ENST00000681659.1:c.3821A>C
|
ENSP00000505631.1:p.Lys1274Thr
|
|
ENST00000355832.9:c.3980A>C
|
ENSP00000348089.5:p.Lys1327Thr
|
|
ENST00000465653.1:n.302A>C
|
|
|
ENST00000623073.3:c.*2276A>C
|
ENSP00000485650.1:n.*2276A>C
|
|
ENST00000623115.3:c.2090A>C
|
ENSP00000485321.1:p.Lys697Thr
|
|
ENST00000624341.3:c.1812A>C
|
|
|
NM_000124.3:c.3980A>C
|
NP_000115.1:p.Lys1327Thr
|
|
XR_945953.1:n.243-10210T>G
|
|
|
NM_001346440.1:c.3980A>C
|
NP_001333369.1:p.Lys1327Thr
|
|
NM_000124.4:c.3980A>C
MANE Select
|
NP_000115.1:p.Lys1327Thr
|
|
NM_001346440.2:c.3980A>C
|
NP_001333369.1:p.Lys1327Thr
|
|