ENST00000299314.12:c.3391T>G
MANE Select
|
ENSP00000299314.7:p.Ser1131Ala
|
|
ENST00000299314.11:c.3391T>G
|
ENSP00000299314.7:p.Ser1131Ala
|
|
ENST00000549194.1:n.257T>G
|
|
|
ENST00000549738.5:c.142T>G
|
ENSP00000450161.1:p.Ser48Ala
|
|
ENST00000550718.1:c.203T>G
|
|
|
NM_024312.4:c.3391T>G
|
NP_077288.2:p.Ser1131Ala
|
|
XM_006719593.2:c.3391T>G
|
XP_006719656.1:p.Ser1131Ala
|
|
XM_011538731.1:c.3310T>G
|
XP_011537033.1:p.Ser1104Ala
|
|
XM_006719593.3:c.3391T>G
|
XP_006719656.1:p.Ser1131Ala
|
|
XM_011538731.2:c.3310T>G
|
XP_011537033.1:p.Ser1104Ala
|
|
XM_017019961.1:c.3175T>G
|
XP_016875450.1:p.Ser1059Ala
|
|
XM_017019962.2:c.2164T>G
|
XP_016875451.1:p.Ser722Ala
|
|
NM_024312.5:c.3391T>G
MANE Select
|
NP_077288.2:p.Ser1131Ala
|
|