ENST00000355832.10:c.3938C>A
MANE Select
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ENSP00000348089.5:p.Thr1313Asn
|
|
ENST00000679552.1:n.1009C>A
|
|
|
ENST00000679871.1:n.1084C>A
|
|
|
ENST00000679974.1:n.987C>A
|
|
|
ENST00000681632.1:n.5341C>A
|
|
|
ENST00000681659.1:c.3779C>A
|
ENSP00000505631.1:p.Thr1260Asn
|
|
ENST00000355832.9:c.3938C>A
|
ENSP00000348089.5:p.Thr1313Asn
|
|
ENST00000465653.1:n.260C>A
|
|
|
ENST00000623073.3:c.*2234C>A
|
ENSP00000485650.1:n.*2234C>A
|
|
ENST00000623115.3:c.2048C>A
|
ENSP00000485321.1:p.Thr683Asn
|
|
ENST00000624341.3:c.1770C>A
|
|
|
NM_000124.3:c.3938C>A
|
NP_000115.1:p.Thr1313Asn
|
|
XR_945953.1:n.243-10168G>T
|
|
|
NM_001346440.1:c.3938C>A
|
NP_001333369.1:p.Thr1313Asn
|
|
NM_000124.4:c.3938C>A
MANE Select
|
NP_000115.1:p.Thr1313Asn
|
|
NM_001346440.2:c.3938C>A
|
NP_001333369.1:p.Thr1313Asn
|
|