ENST00000539696.6:c.127G>T
|
ENSP00000439134.1:p.Ala43Ser
|
|
ENST00000546277.6:c.970G>T
|
ENSP00000438153.2:p.Ala324Ser
|
|
ENST00000636529.2:n.609G>T
|
|
|
ENST00000697195.1:c.*734G>T
|
ENSP00000513181.1:n.*734G>T
|
|
ENST00000697196.1:c.*143G>T
|
ENSP00000513182.1:n.*143G>T
|
|
ENST00000697197.1:n.2999G>T
|
|
|
ENST00000697198.1:n.1354G>T
|
|
|
ENST00000228510.8:c.970G>T
MANE Select
|
ENSP00000228510.3:p.Ala324Ser
|
|
ENST00000636529.1:c.595G>T
|
|
|
ENST00000636996.1:c.818G>T
|
|
|
ENST00000228510.7:c.970G>T
|
ENSP00000228510.3:p.Ala324Ser
|
|
ENST00000392727.7:c.814G>T
|
ENSP00000376487.3:p.Ala272Ser
|
|
ENST00000447878.6:c.*417G>T
|
ENSP00000415555.2:n.*417G>T
|
|
ENST00000537237.5:c.*643G>T
|
ENSP00000445382.1:n.*643G>T
|
|
ENST00000539575.4:c.970G>T
|
ENSP00000443551.2:p.Ala324Ser
|
|
ENST00000539696.5:c.127G>T
|
ENSP00000439134.1:p.Ala43Ser
|
|
ENST00000540353.1:n.3203G>T
|
|
|
ENST00000625889.2:c.814G>T
|
ENSP00000486846.1:p.Ala272Ser
|
|
ENST00000629016.2:c.*417G>T
|
ENSP00000486804.1:n.*417G>T
|
|
NM_000431.3:c.970G>T
|
NP_000422.1:p.Ala324Ser
|
|
NM_001114185.2:c.970G>T
|
NP_001107657.1:p.Ala324Ser
|
|
NM_001301182.1:c.814G>T
|
NP_001288111.1:p.Ala272Ser
|
|
XM_011538372.1:c.970G>T
|
XP_011536674.1:p.Ala324Ser
|
|
XM_017019313.2:c.814G>T
|
XP_016874802.1:p.Ala272Ser
|
|
XM_017019314.1:c.970G>T
|
XP_016874803.1:p.Ala324Ser
|
|
NM_000431.4:c.970G>T
MANE Select
|
NP_000422.1:p.Ala324Ser
|
|
NM_001114185.3:c.970G>T
|
NP_001107657.1:p.Ala324Ser
|
|
NM_001301182.2:c.814G>T
|
NP_001288111.1:p.Ala272Ser
|
|