ENST00000355832.10:c.3812T>G
MANE Select
|
ENSP00000348089.5:p.Ile1271Ser
|
|
ENST00000679552.1:n.883T>G
|
|
|
ENST00000679871.1:n.958T>G
|
|
|
ENST00000679974.1:n.861T>G
|
|
|
ENST00000681632.1:n.5215T>G
|
|
|
ENST00000681659.1:c.3653T>G
|
ENSP00000505631.1:p.Ile1218Ser
|
|
ENST00000355832.9:c.3812T>G
|
ENSP00000348089.5:p.Ile1271Ser
|
|
ENST00000465653.1:n.134T>G
|
|
|
ENST00000623073.3:c.*2108T>G
|
ENSP00000485650.1:n.*2108T>G
|
|
ENST00000623115.3:c.1922T>G
|
ENSP00000485321.1:p.Ile641Ser
|
|
ENST00000624341.3:c.1644T>G
|
|
|
NM_000124.3:c.3812T>G
|
NP_000115.1:p.Ile1271Ser
|
|
XR_945953.1:n.243-10042A>C
|
|
|
NM_001346440.1:c.3812T>G
|
NP_001333369.1:p.Ile1271Ser
|
|
NM_000124.4:c.3812T>G
MANE Select
|
NP_000115.1:p.Ile1271Ser
|
|
NM_001346440.2:c.3812T>G
|
NP_001333369.1:p.Ile1271Ser
|
|