ENST00000267890.11:c.1409+18T>C
MANE Select
|
ENSP00000267890.6:n.1409+18T>C
|
|
ENST00000267890.10:c.1409+18T>C
|
ENSP00000267890.6:n.1409+18T>C
|
|
ENST00000567274.5:c.1322T>C
|
ENSP00000457489.1:p.Phe441Ser
|
|
ENST00000567840.5:c.1427T>C
|
ENSP00000455734.1:p.Phe476Ser
|
|
ENST00000622375.4:c.2624+18T>C
|
ENSP00000479984.1:n.2624+18T>C
|
|
NM_173500.3:c.1409+18T>C
|
NP_775771.3:n.1409+18T>C
|
|
XM_005254171.3:c.1427+18T>C
|
XP_005254228.1:n.1427+18T>C
|
|
XM_005254173.3:c.1202+18T>C
|
XP_005254230.1:n.1202+18T>C
|
|
XM_006720402.2:c.1394+18T>C
|
XP_006720465.1:n.1394+18T>C
|
|
XM_006720403.2:c.1202+18T>C
|
XP_006720466.1:n.1202+18T>C
|
|
XM_011521267.1:c.1202+18T>C
|
XP_011519569.1:n.1202+18T>C
|
|
XM_011521268.1:c.1142+18T>C
|
XP_011519570.1:n.1142+18T>C
|
|
XM_011521269.1:c.1130+18T>C
|
XP_011519571.1:n.1130+18T>C
|
|
XM_005254171.5:c.1427+18T>C
|
XP_005254228.1:n.1427+18T>C
|
|
XM_005254173.5:c.1202+18T>C
|
XP_005254230.1:n.1202+18T>C
|
|
XM_006720402.4:c.1394+18T>C
|
XP_006720465.1:n.1394+18T>C
|
|
XM_006720403.4:c.1202+18T>C
|
XP_006720466.1:n.1202+18T>C
|
|
XM_017021950.2:c.1130+18T>C
|
XP_016877439.1:n.1130+18T>C
|
|
XM_024449849.1:c.1409+18T>C
|
XP_024305617.1:n.1409+18T>C
|
|
XM_024449850.1:c.1409+18T>C
|
XP_024305618.1:n.1409+18T>C
|
|
XM_024449851.1:c.1202+18T>C
|
XP_024305619.1:n.1202+18T>C
|
|
NM_173500.4:c.1409+18T>C
MANE Select
|
NP_775771.3:n.1409+18T>C
|
|