ENST00000307712.11:c.1138T>G
MANE Select
|
ENSP00000306881.6:p.Ser380Ala
|
|
ENST00000307712.10:c.1138T>G
|
ENSP00000306881.6:p.Ser380Ala
|
|
ENST00000537403.5:c.532T>G
|
ENSP00000444193.1:p.Ser178Ala
|
|
ENST00000545328.6:c.1051T>G
|
ENSP00000445393.2:p.Ser351Ala
|
|
NM_006364.2:c.1138T>G
|
NP_006355.2:p.Ser380Ala
|
|
XM_005267262.1:c.1138T>G
|
XP_005267319.1:p.Ser380Ala
|
|
XM_011536355.1:c.1138T>G
|
XP_011534657.1:p.Ser380Ala
|
|
NM_006364.3:c.1138T>G
|
NP_006355.2:p.Ser380Ala
|
|
XM_005267262.2:c.1138T>G
|
XP_005267319.1:p.Ser380Ala
|
|
XM_011536355.3:c.1138T>G
|
XP_011534657.1:p.Ser380Ala
|
|
XM_017020928.2:c.1138T>G
|
XP_016876417.1:p.Ser380Ala
|
|
NM_006364.4:c.1138T>G
MANE Select
|
NP_006355.2:p.Ser380Ala
|
|