ENST00000576204.6:n.789C>G
|
|
|
ENST00000622290.5:c.*98C>G
|
ENSP00000483331.2:n.*98C>G
|
|
ENST00000205557.12:c.3926C>G
MANE Select
|
ENSP00000205557.7:p.Ala1309Gly
|
|
ENST00000640696.1:c.740C>G
|
ENSP00000492197.1:p.Ala247Gly
|
|
ENST00000205557.11:c.3926C>G
|
ENSP00000205557.7:p.Ala1309Gly
|
|
ENST00000456970.6:c.3551C>G
|
ENSP00000405002.2:n.3551C>G
|
|
ENST00000576204.5:n.789C>G
|
|
|
ENST00000622290.4:c.*1135C>G
|
ENSP00000483331.1:n.*1135C>G
|
|
NM_001171.5:c.3926C>G
|
NP_001162.4:p.Ala1309Gly
|
|
XM_011522479.1:c.3893C>G
|
XP_011520781.1:p.Ala1298Gly
|
|
XM_011522480.1:c.3584C>G
|
XP_011520782.1:p.Ala1195Gly
|
|
XM_011522481.1:c.3584C>G
|
XP_011520783.1:p.Ala1195Gly
|
|
XR_932836.1:n.4224C>G
|
|
|
XR_932837.1:n.3962C>G
|
|
|
XR_932838.1:n.4025C>G
|
|
|
XR_933134.1:n.539-4793G>C
|
|
|
NM_001351800.1:c.3584C>G
|
NP_001338729.1:p.Ala1195Gly
|
|
NR_147784.1:n.3588C>G
|
|
|
XM_011522479.2:c.3893C>G
|
XP_011520781.1:p.Ala1298Gly
|
|
XM_011522481.3:c.3584C>G
|
XP_011520783.1:p.Ala1195Gly
|
|
XM_017023212.1:c.3758C>G
|
XP_016878701.1:p.Ala1253Gly
|
|
XM_024450261.1:c.3962C>G
|
XP_024306029.1:p.Ala1321Gly
|
|
XR_932836.2:n.4170C>G
|
|
|
XR_932837.3:n.3907C>G
|
|
|
XR_932838.3:n.3970C>G
|
|
|
NM_001171.6:c.3926C>G
MANE Select
|
NP_001162.5:p.Ala1309Gly
|
|