NM_006521.6:c.1701C>G
MANE Select
|
NP_006512.2:p.Ser567Arg
|
ENST00000315869.8:c.1701C>G
MANE Select
|
ENSP00000314129.7:p.Ser567Arg
|
NM_001282142.1:c.1386C>G
|
NP_001269071.1:p.Ser462Arg
|
NM_001282142.2:c.1386C>G
|
NP_001269071.1:p.Ser462Arg
|
NM_006521.5:c.1701C>G
|
NP_006512.2:p.Ser567Arg
|
ENST00000315869.7:c.1701C>G
|
ENSP00000314129.7:p.Ser567Arg
|
ENST00000493583.5:c.*1306C>G
|
ENSP00000476976.1:n.*1306C>G
|
XM_006724549.2:c.1386C>G
|
XP_006724612.1:p.Ser462Arg
|
XM_011543952.1:c.*331C>G
|
XP_011542254.1:n.*331C>G
|
XM_024452432.1:c.*331C>G
|
XP_024308200.1:n.*331C>G
|