ENST00000589419.2:n.985T>G
|
|
|
ENST00000650467.2:c.760T>G
|
ENSP00000496897.2:p.Ser254Ala
|
|
ENST00000695903.1:c.1095T>G
|
ENSP00000512255.1:p.Gly365=
|
|
ENST00000695904.1:c.1095T>G
|
ENSP00000512259.1:p.Gly365=
|
|
ENST00000439986.9:c.982T>G
MANE Select
|
ENSP00000404464.2:p.Ser328Ala
|
|
ENST00000589116.2:n.690T>G
|
|
|
ENST00000649564.1:c.982T>G
|
ENSP00000497183.1:p.Ser328Ala
|
|
ENST00000650467.1:c.638T>G
|
|
|
ENST00000398179.3:c.772T>G
|
ENSP00000381241.3:p.Ser258Ala
|
|
ENST00000439986.8:c.982T>G
|
ENSP00000404464.2:p.Ser328Ala
|
|
ENST00000589116.1:n.690T>G
|
|
|
NM_133459.3:c.982T>G
|
NP_597716.1:p.Ser328Ala
|
|
XM_005266648.2:c.982T>G
|
XP_005266705.1:p.Ser328Ala
|
|
NM_133459.4:c.982T>G
MANE Select
|
NP_597716.1:p.Ser328Ala
|
|
XM_017025556.1:c.1095T>G
|
XP_016881045.1:p.Gly365=
|
|
XM_017025557.1:c.1095T>G
|
XP_016881046.1:p.Gly365=
|
|
XM_017025558.1:c.982T>G
|
XP_016881047.1:p.Ser328Ala
|
|
XM_024451091.1:c.982T>G
|
XP_024306859.1:p.Ser328Ala
|
|
XR_001753142.1:n.1934T>G
|
|
|