ENST00000256906.5:c.498T>G
MANE Select
|
ENSP00000256906.4:p.Pro166=
|
|
ENST00000256906.4:c.498T>G
|
ENSP00000256906.4:p.Pro166=
|
|
ENST00000426880.2:c.234T>G
|
ENSP00000402526.2:p.Pro78=
|
|
NM_001143828.1:c.234T>G
|
NP_001137300.1:p.Pro78=
|
|
NM_001160166.1:c.*130T>G
|
NP_001153638.1:n.*130T>G
|
|
NM_021624.3:c.498T>G
|
NP_067637.2:p.Pro166=
|
|
XM_011526133.1:c.357+7936T>G
|
XP_011524435.1:n.357+7936T>G
|
|
NM_021624.4:c.498T>G
MANE Select
|
NP_067637.2:p.Pro166=
|
|
NM_001143828.2:c.234T>G
|
NP_001137300.1:p.Pro78=
|
|
NM_001160166.2:c.*130T>G
|
NP_001153638.1:n.*130T>G
|
|