ENST00000696142.1:c.*246A>C
|
ENSP00000512434.1:n.*246A>C
|
|
ENST00000696143.1:c.705A>C
|
ENSP00000512435.1:n.705A>C
|
|
ENST00000696153.1:c.680A>C
|
ENSP00000512444.1:p.Asp227Ala
|
|
ENST00000256474.3:c.569A>C
MANE Select
|
ENSP00000256474.3:p.Asp190Ala
|
|
ENST00000256474.2:c.569A>C
|
ENSP00000256474.2:p.Asp190Ala
|
|
ENST00000345392.2:c.446A>C
|
ENSP00000344757.2:p.Asp149Ala
|
|
ENST00000477538.1:n.705A>C
|
|
|
NM_000551.3:c.569A>C , LRG_322t1:c.569A>C
|
NP_000542.1:p.Asp190Ala
|
|
NM_198156.2:c.446A>C
|
NP_937799.1:p.Asp149Ala
|
|
NM_001354723.1:c.*123A>C
|
NP_001341652.1:n.*123A>C
|
|
NM_000551.4:c.569A>C
MANE Select
|
NP_000542.1:p.Asp190Ala
|
|
NM_001354723.2:c.*123A>C
|
NP_001341652.1:n.*123A>C
|
|
NM_198156.3:c.446A>C
|
NP_937799.1:p.Asp149Ala
|
|