ENST00000355832.10:c.3902G>T
MANE Select
|
ENSP00000348089.5:p.Arg1301Leu
|
|
ENST00000679552.1:n.973G>T
|
|
|
ENST00000679871.1:n.1048G>T
|
|
|
ENST00000679974.1:n.951G>T
|
|
|
ENST00000681632.1:n.5305G>T
|
|
|
ENST00000681659.1:c.3743G>T
|
ENSP00000505631.1:p.Arg1248Leu
|
|
ENST00000355832.9:c.3902G>T
|
ENSP00000348089.5:p.Arg1301Leu
|
|
ENST00000465653.1:n.224G>T
|
|
|
ENST00000623073.3:c.*2198G>T
|
ENSP00000485650.1:n.*2198G>T
|
|
ENST00000623115.3:c.2012G>T
|
ENSP00000485321.1:p.Arg671Leu
|
|
ENST00000624341.3:c.1734G>T
|
|
|
NM_000124.3:c.3902G>T
|
NP_000115.1:p.Arg1301Leu
|
|
XR_945953.1:n.243-10132C>A
|
|
|
NM_001346440.1:c.3902G>T
|
NP_001333369.1:p.Arg1301Leu
|
|
NM_000124.4:c.3902G>T
MANE Select
|
NP_000115.1:p.Arg1301Leu
|
|
NM_001346440.2:c.3902G>T
|
NP_001333369.1:p.Arg1301Leu
|
|