ENST00000298910.12:c.6061G>T
MANE Select
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ENSP00000298910.7:p.Ala2021Ser
|
|
ENST00000679360.1:c.*4970G>T
|
ENSP00000505368.1:n.*4970G>T
|
|
ENST00000679532.1:c.1835G>T
|
|
|
ENST00000680018.1:c.1506G>T
|
ENSP00000505347.1:n.1506G>T
|
|
ENST00000680422.1:c.1706G>T
|
|
|
ENST00000680425.1:c.1228G>T
|
ENSP00000506459.1:n.1228G>T
|
|
ENST00000680453.1:c.1518G>T
|
|
|
ENST00000680790.1:c.5806G>T
|
ENSP00000505335.1:p.Ala1936Ser
|
|
ENST00000681136.1:n.2045G>T
|
|
|
ENST00000681696.1:c.1744G>T
|
ENSP00000505871.1:p.Ala582Ser
|
|
ENST00000298910.11:c.6061G>T
|
ENSP00000298910.7:p.Ala2021Ser
|
|
ENST00000430804.5:c.3357G>T
|
|
|
ENST00000479187.5:n.2742G>T
|
|
|
NM_198578.3:c.6061G>T
|
NP_940980.3:p.Ala2021Ser
|
|
XM_005268629.2:c.6061G>T
|
XP_005268686.1:p.Ala2021Ser
|
|
XM_011537877.1:c.6061G>T
|
XP_011536179.1:p.Ala2021Ser
|
|
XM_011537878.1:c.6061G>T
|
XP_011536180.1:p.Ala2021Ser
|
|
XM_011537879.1:c.4858G>T
|
XP_011536181.1:p.Ala1620Ser
|
|
XM_005268629.4:c.6061G>T
|
XP_005268686.1:p.Ala2021Ser
|
|
XM_011537877.3:c.6061G>T
|
XP_011536179.1:p.Ala2021Ser
|
|
XM_017018787.1:c.2977G>T
|
XP_016874276.1:p.Ala993Ser
|
|
XM_017018788.2:c.2323G>T
|
XP_016874277.1:p.Ala775Ser
|
|
XM_024448833.1:c.4858G>T
|
XP_024304601.1:p.Ala1620Ser
|
|
NM_198578.4:c.6061G>T
MANE Select
|
NP_940980.4:p.Ala2021Ser
|
|