ENST00000393564.7:c.994T>G
|
ENSP00000377194.2:p.Ser332Ala
|
|
ENST00000439227.6:c.997T>G
|
ENSP00000395599.2:p.Ser333Ala
|
|
ENST00000696420.1:c.994T>G
|
ENSP00000512615.1:p.Ser332Ala
|
|
ENST00000696421.1:c.994T>G
|
ENSP00000512616.1:p.Ser332Ala
|
|
ENST00000696422.1:c.857T>G
|
|
|
ENST00000696423.1:c.860T>G
|
|
|
ENST00000696424.1:c.846T>G
|
ENSP00000512619.1:n.846T>G
|
|
ENST00000696425.1:c.865-197T>G
|
ENSP00000512620.1:n.865-197T>G
|
|
ENST00000696426.1:c.*454T>G
|
ENSP00000512621.1:n.*454T>G
|
|
ENST00000696427.1:c.1001T>G
|
ENSP00000512622.1:p.Val334Gly
|
|
ENST00000696428.1:c.*836T>G
|
ENSP00000512623.1:n.*836T>G
|
|
ENST00000696429.1:c.994T>G
|
ENSP00000512624.1:p.Ser332Ala
|
|
ENST00000696430.1:c.994T>G
|
ENSP00000512625.1:p.Ser332Ala
|
|
ENST00000393562.10:c.994T>G
MANE Select
|
ENSP00000377192.3:p.Ser332Ala
|
|
ENST00000369620.6:c.1132T>G
|
ENSP00000358633.2:p.Ser378Ala
|
|
ENST00000393562.6:c.1084T>G
|
ENSP00000377192.2:p.Ser362Ala
|
|
ENST00000393564.6:c.994T>G
|
ENSP00000377194.2:p.Ser332Ala
|
|
ENST00000439227.5:c.997T>G
|
ENSP00000395599.1:p.Ser333Ala
|
|
ENST00000490651.1:n.76T>G
|
|
|
ENST00000621232.4:c.994T>G
|
ENSP00000483686.1:p.Ser332Ala
|
|
NM_000402.4:c.1084T>G
|
NP_000393.4:p.Ser362Ala
|
|
NM_001042351.2:c.994T>G
|
NP_001035810.1:p.Ser332Ala
|
|
XM_005274657.2:c.1087T>G
|
XP_005274714.1:p.Ser363Ala
|
|
XM_005274658.2:c.997T>G
|
XP_005274715.1:p.Ser333Ala
|
|
XM_011531132.1:c.958-197T>G
|
XP_011529434.1:n.958-197T>G
|
|
NM_001360016.2:c.994T>G
MANE Select
|
NP_001346945.1:p.Ser332Ala
|
|
NM_001042351.3:c.994T>G
|
NP_001035810.1:p.Ser332Ala
|
|