ENST00000248633.9:c.340G>C
MANE Select
|
ENSP00000248633.4:p.Asp114His
|
|
ENST00000248633.8:c.340G>C
|
ENSP00000248633.4:p.Asp114His
|
|
ENST00000428214.5:c.340G>C
|
ENSP00000394413.1:p.Asp114His
|
|
ENST00000438045.5:c.273+3090G>C
|
ENSP00000410438.1:n.273+3090G>C
|
|
ENST00000484913.5:n.344G>C
|
|
|
NM_000466.2:c.340G>C
|
NP_000457.1:p.Asp114His
|
|
NM_001282677.1:c.340G>C
|
NP_001269606.1:p.Asp114His
|
|
NM_001282678.1:c.-320G>C
|
NP_001269607.1:n.-320G>C
|
|
XR_242246.3:n.436G>C
|
|
|
XR_242246.5:n.387G>C
|
|
|
NM_000466.3:c.340G>C
MANE Select
|
NP_000457.1:p.Asp114His
|
|
NM_001282677.2:c.340G>C
|
NP_001269606.1:p.Asp114His
|
|
NM_001282678.2:c.-320G>C
|
NP_001269607.1:n.-320G>C
|
|