ENST00000649046.1:c.2365T>C
MANE Select
|
ENSP00000496870.1:p.Leu789=
|
|
ENST00000263816.7:c.2365T>C
|
ENSP00000263816.3:p.Leu789=
|
|
ENST00000443831.1:c.1954T>C
|
ENSP00000409813.1:p.Leu652=
|
|
NM_004525.2:c.2365T>C
|
NP_004516.2:p.Leu789=
|
|
XM_011511183.1:c.2365T>C
|
XP_011509485.1:p.Leu789=
|
|
XM_011511184.1:c.76T>C
|
XP_011509486.1:p.Leu26=
|
|
XM_011511185.1:c.2365T>C
|
XP_011509487.1:p.Leu789=
|
|
NM_004525.3:c.2365T>C
MANE Select
|
NP_004516.2:p.Leu789=
|
|
XM_011511183.3:c.2365T>C
|
XP_011509485.1:p.Leu789=
|
|
XM_011511184.2:c.76T>C
|
XP_011509486.1:p.Leu26=
|
|