ENST00000539696.6:c.-85G>T
|
ENSP00000439134.1:n.-85G>T
|
|
ENST00000546277.6:c.759G>T
|
ENSP00000438153.2:p.Arg253Ser
|
|
ENST00000636529.2:n.398G>T
|
|
|
ENST00000697195.1:c.*523G>T
|
ENSP00000513181.1:n.*523G>T
|
|
ENST00000697196.1:c.847G>T
|
ENSP00000513182.1:p.Ala283Ser
|
|
ENST00000697197.1:n.2409G>T
|
|
|
ENST00000228510.8:c.759G>T
MANE Select
|
ENSP00000228510.3:p.Arg253Ser
|
|
ENST00000636529.1:c.384G>T
|
|
|
ENST00000636996.1:c.607G>T
|
|
|
ENST00000228510.7:c.759G>T
|
ENSP00000228510.3:p.Arg253Ser
|
|
ENST00000392727.7:c.603G>T
|
ENSP00000376487.3:p.Arg201Ser
|
|
ENST00000447878.6:c.*206G>T
|
ENSP00000415555.2:n.*206G>T
|
|
ENST00000537237.5:c.*442-389G>T
|
ENSP00000445382.1:n.*442-389G>T
|
|
ENST00000539575.4:c.759G>T
|
ENSP00000443551.2:p.Arg253Ser
|
|
ENST00000539696.5:c.-85G>T
|
ENSP00000439134.1:n.-85G>T
|
|
ENST00000540353.1:n.2992G>T
|
|
|
ENST00000625889.2:c.603G>T
|
ENSP00000486846.1:p.Arg201Ser
|
|
ENST00000629016.2:c.*206G>T
|
ENSP00000486804.1:n.*206G>T
|
|
NM_000431.3:c.759G>T
|
NP_000422.1:p.Arg253Ser
|
|
NM_001114185.2:c.759G>T
|
NP_001107657.1:p.Arg253Ser
|
|
NM_001301182.1:c.603G>T
|
NP_001288111.1:p.Arg201Ser
|
|
XM_011538372.1:c.759G>T
|
XP_011536674.1:p.Arg253Ser
|
|
XM_017019313.2:c.603G>T
|
XP_016874802.1:p.Arg201Ser
|
|
XM_017019314.1:c.759G>T
|
XP_016874803.1:p.Arg253Ser
|
|
XM_024448982.1:c.759G>T
|
XP_024304750.1:p.Arg253Ser
|
|
NM_000431.4:c.759G>T
MANE Select
|
NP_000422.1:p.Arg253Ser
|
|
NM_001114185.3:c.759G>T
|
NP_001107657.1:p.Arg253Ser
|
|
NM_001301182.2:c.603G>T
|
NP_001288111.1:p.Arg201Ser
|
|