ENST00000356839.10:c.1455T>G
MANE Select
|
ENSP00000349297.5:p.Ser485=
|
|
ENST00000322910.9:c.*1410T>G
|
ENSP00000325395.5:n.*1410T>G
|
|
ENST00000350303.9:c.1389T>G
|
ENSP00000344152.5:p.Ser463=
|
|
ENST00000356839.9:c.1455T>G
|
ENSP00000349297.5:p.Ser485=
|
|
ENST00000542255.6:c.313T>G
|
|
|
ENST00000543245.6:c.1524T>G
|
ENSP00000438689.2:p.Ser508=
|
|
ENST00000578711.1:n.662T>G
|
|
|
ENST00000579391.1:n.63T>G
|
|
|
ENST00000579425.5:n.571T>G
|
|
|
ENST00000579546.1:c.271+97T>G
|
|
|
ENST00000579894.5:n.242T>G
|
|
|
ENST00000583074.5:n.153+97T>G
|
|
|
ENST00000583850.5:n.230T>G
|
|
|
ENST00000583858.5:c.463+97T>G
|
|
|
ENST00000585203.6:n.646T>G
|
|
|
NM_000018.3:c.1455T>G
|
NP_000009.1:p.Ser485=
|
|
NM_001033859.2:c.1389T>G
|
NP_001029031.1:p.Ser463=
|
|
NM_001270447.1:c.1524T>G
|
NP_001257376.1:p.Ser508=
|
|
NM_001270448.1:c.1227T>G
|
NP_001257377.1:p.Ser409=
|
|
XM_006721516.2:c.1455T>G
|
XP_006721579.2:p.Ser485=
|
|
XM_011523829.1:c.1434+97T>G
|
XP_011522131.1:n.1434+97T>G
|
|
XM_011523830.1:c.1434+97T>G
|
XP_011522132.1:n.1434+97T>G
|
|
XR_934021.1:n.1562T>G
|
|
|
XR_934022.1:n.1541+97T>G
|
|
|
XR_934023.1:n.1541+97T>G
|
|
|
XM_006721516.3:c.1455T>G
|
XP_006721579.2:p.Ser485=
|
|
XM_011523829.2:c.1434+97T>G
|
XP_011522131.1:n.1434+97T>G
|
|
XM_011523830.2:c.1434+97T>G
|
XP_011522132.1:n.1434+97T>G
|
|
XM_024450741.1:c.1434+97T>G
|
XP_024306509.1:n.1434+97T>G
|
|
XR_934021.2:n.1514T>G
|
|
|
XR_934022.2:n.1493+97T>G
|
|
|
XR_934023.2:n.1493+97T>G
|
|
|
NM_000018.4:c.1455T>G
MANE Select
|
NP_000009.1:p.Ser485=
|
|
NM_001033859.3:c.1389T>G
|
NP_001029031.1:p.Ser463=
|
|
NM_001270447.2:c.1524T>G
|
NP_001257376.1:p.Ser508=
|
|
NM_001270448.2:c.1227T>G
|
NP_001257377.1:p.Ser409=
|
|