ENST00000355832.10:c.2934C>T
MANE Select
|
ENSP00000348089.5:p.Phe978=
|
|
ENST00000679552.1:n.142-222C>T
|
|
|
ENST00000679871.1:n.80C>T
|
|
|
ENST00000679974.1:n.120-222C>T
|
|
|
ENST00000681632.1:n.4337C>T
|
|
|
ENST00000681659.1:c.2775C>T
|
ENSP00000505631.1:p.Phe925=
|
|
ENST00000355832.9:c.2934C>T
|
ENSP00000348089.5:p.Phe978=
|
|
ENST00000623073.3:c.*1230C>T
|
ENSP00000485650.1:n.*1230C>T
|
|
ENST00000623115.3:c.1044C>T
|
ENSP00000485321.1:p.Phe348=
|
|
ENST00000624341.3:c.766C>T
|
|
|
NM_000124.3:c.2934C>T
|
NP_000115.1:p.Phe978=
|
|
XR_945953.1:n.243-454G>A
|
|
|
NM_001346440.1:c.2934C>T
|
NP_001333369.1:p.Phe978=
|
|
NM_000124.4:c.2934C>T
MANE Select
|
NP_000115.1:p.Phe978=
|
|
NM_001346440.2:c.2934C>T
|
NP_001333369.1:p.Phe978=
|
|