ENST00000573725.2:c.6521G>C
|
ENSP00000460849.2:p.Gly2174Ala
|
|
ENST00000703537.1:c.2449G>C
|
|
|
ENST00000703538.1:c.*6424G>C
|
ENSP00000515361.1:n.*6424G>C
|
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ENST00000703539.1:n.3015G>C
|
|
|
ENST00000703540.1:c.6554G>C
|
ENSP00000515362.1:p.Gly2185Ala
|
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ENST00000703541.1:c.6566G>C
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ENSP00000515363.1:p.Gly2189Ala
|
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ENST00000304992.11:c.6701G>C
MANE Select
|
ENSP00000304350.6:p.Gly2234Ala
|
|
ENST00000304992.10:c.6701G>C
|
ENSP00000304350.6:p.Gly2234Ala
|
|
ENST00000571958.1:c.10G>C
|
|
|
ENST00000572621.5:c.6701G>C
|
ENSP00000460348.1:p.Gly2234Ala
|
|
ENST00000572723.1:n.690G>C
|
|
|
NM_006445.3:c.6701G>C
|
NP_006436.3:p.Gly2234Ala
|
|
XM_024450537.1:c.6701G>C
|
XP_024306305.1:p.Gly2234Ala
|
|
NM_006445.4:c.6701G>C
MANE Select
|
NP_006436.3:p.Gly2234Ala
|
|