|
NM_002615.7:c.907C>T
MANE Select
|
NP_002606.3:p.Arg303Ter
|
|
ENST00000254722.9:c.907C>T
MANE Select
|
ENSP00000254722.4:p.Arg303Ter
|
|
NM_001329903.1:c.907C>T
|
NP_001316832.1:p.Arg303Ter
|
|
NM_001329903.2:c.907C>T
|
NP_001316832.1:p.Arg303Ter
|
|
NM_001329904.1:c.346C>T
|
NP_001316833.1:p.Arg116Ter
|
|
NM_001329904.2:c.346C>T
|
NP_001316833.1:p.Arg116Ter
|
|
NM_001329905.1:c.346C>T
|
NP_001316834.1:p.Arg116Ter
|
|
NM_001329905.2:c.346C>T
|
NP_001316834.1:p.Arg116Ter
|
|
NM_002615.5:c.907C>T
|
NP_002606.3:p.Arg303Ter
|
|
NM_002615.6:c.907C>T
|
NP_002606.3:p.Arg303Ter
|
|
ENST00000254722.8:c.907C>T
|
ENSP00000254722.4:p.Arg303Ter
|
|
ENST00000572517.1:n.203C>T
|
|
|
ENST00000573763.1:c.301C>T
|
ENSP00000461405.1:p.Arg101Ter
|