ENST00000355832.10:c.3584C>A
MANE Select
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ENSP00000348089.5:p.Thr1195Asn
|
|
ENST00000679552.1:n.655C>A
|
|
|
ENST00000679871.1:n.730C>A
|
|
|
ENST00000679974.1:n.633C>A
|
|
|
ENST00000681632.1:n.4987C>A
|
|
|
ENST00000681659.1:c.3425C>A
|
ENSP00000505631.1:p.Thr1142Asn
|
|
ENST00000355832.9:c.3584C>A
|
ENSP00000348089.5:p.Thr1195Asn
|
|
ENST00000623073.3:c.*1880C>A
|
ENSP00000485650.1:n.*1880C>A
|
|
ENST00000623115.3:c.1694C>A
|
ENSP00000485321.1:p.Thr565Asn
|
|
ENST00000624341.3:c.1416C>A
|
|
|
NM_000124.3:c.3584C>A
|
NP_000115.1:p.Thr1195Asn
|
|
XR_945953.1:n.243-1189G>T
|
|
|
NM_001346440.1:c.3584C>A
|
NP_001333369.1:p.Thr1195Asn
|
|
NM_000124.4:c.3584C>A
MANE Select
|
NP_000115.1:p.Thr1195Asn
|
|
NM_001346440.2:c.3584C>A
|
NP_001333369.1:p.Thr1195Asn
|
|