ENST00000682114.1:c.229C>G
|
ENSP00000507245.1:p.Pro77Ala
|
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ENST00000682478.1:n.205C>G
|
|
|
ENST00000683576.1:n.205C>G
|
|
|
ENST00000683627.1:c.229C>G
|
ENSP00000507533.1:p.Pro77Ala
|
|
ENST00000684082.1:c.229C>G
|
ENSP00000508266.1:p.Pro77Ala
|
|
ENST00000684633.1:n.201C>G
|
|
|
ENST00000684678.1:c.225C>G
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ENSP00000507059.1:n.225C>G
|
|
ENST00000369842.9:c.229C>G
MANE Select
|
ENSP00000358857.4:p.Pro77Ala
|
|
ENST00000369835.3:c.124C>G
|
ENSP00000358850.3:p.Pro42Ala
|
|
ENST00000369842.8:c.229C>G
|
ENSP00000358857.4:p.Pro77Ala
|
|
ENST00000428228.5:c.*134C>G
|
ENSP00000401081.1:n.*134C>G
|
|
ENST00000468294.5:n.189C>G
|
|
|
ENST00000485261.1:n.205C>G
|
|
|
ENST00000486738.5:n.373C>G
|
|
|
ENST00000492448.1:n.212C>G
|
|
|
ENST00000494443.5:n.286C>G
|
|
|
NM_000117.2:c.229C>G , LRG_745t1:c.229C>G
|
NP_000108.1:p.Pro77Ala
|
|
XM_024452349.1:c.21C>G
|
XP_024308117.1:p.Phe7Leu
|
|
NM_000117.3:c.229C>G
MANE Select
|
NP_000108.1:p.Pro77Ala
|
|