ENST00000295754.10:c.978C>G
MANE Select
|
ENSP00000295754.5:p.Ala326=
|
|
ENST00000672866.1:n.2574C>G
|
|
|
ENST00000295754.9:c.978C>G
|
ENSP00000295754.5:p.Ala326=
|
|
ENST00000359013.4:c.1053C>G
|
ENSP00000351905.4:p.Ala351=
|
|
NM_001024847.2:c.1053C>G , LRG_779t1:c.1053C>G
|
NP_001020018.1:p.Ala351=
|
|
NM_003242.5:c.978C>G
|
NP_003233.4:p.Ala326=
|
|
XM_011534043.1:c.1005C>G
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XP_011532345.1:p.Ala335=
|
|
XM_011534044.1:c.930C>G
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XP_011532346.1:p.Ala310=
|
|
XM_011534045.1:c.873C>G
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XP_011532347.1:p.Ala291=
|
|
XM_011534043.2:c.1005C>G
|
XP_011532345.1:p.Ala335=
|
|
XM_011534045.3:c.873C>G
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XP_011532347.1:p.Ala291=
|
|
XM_017007106.1:c.873C>G
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XP_016862595.1:p.Ala291=
|
|
NM_003242.6:c.978C>G
MANE Select
|
NP_003233.4:p.Ala326=
|
|