ENST00000344624.8:c.2682+191C>T
MANE Select
|
ENSP00000339845.3:n.2682+191C>T
|
|
ENST00000344624.7:c.2682+191C>T
|
ENSP00000339845.3:n.2682+191C>T
|
|
ENST00000442743.5:c.2571+191C>T
|
ENSP00000409335.1:n.2571+191C>T
|
|
ENST00000505601.5:n.409+191C>T
|
|
|
ENST00000507174.1:n.521+191C>T
|
|
|
ENST00000511367.6:c.2682+191C>T
|
ENSP00000425979.2:n.2682+191C>T
|
|
ENST00000513349.5:c.2571+191C>T
|
ENSP00000424161.1:n.2571+191C>T
|
|
NM_001100412.1:c.2571+191C>T
|
NP_001093882.1:n.2571+191C>T
|
|
NM_013235.4:c.2682+191C>T
|
NP_037367.3:n.2682+191C>T
|
|
XM_005248291.2:c.2682+191C>T
|
XP_005248348.1:n.2682+191C>T
|
|
XM_005248292.2:c.2658+191C>T
|
XP_005248349.1:n.2658+191C>T
|
|
XM_005248293.2:c.2589+191C>T
|
XP_005248350.1:n.2589+191C>T
|
|
XM_005248294.2:c.2478+191C>T
|
XP_005248351.1:n.2478+191C>T
|
|
XM_011514033.1:c.2682+191C>T
|
XP_011512335.1:n.2682+191C>T
|
|
XM_005248291.4:c.2682+191C>T
|
XP_005248348.1:n.2682+191C>T
|
|
XM_005248292.4:c.2658+191C>T
|
XP_005248349.1:n.2658+191C>T
|
|
XM_005248293.4:c.2589+191C>T
|
XP_005248350.1:n.2589+191C>T
|
|
XM_005248294.4:c.2478+191C>T
|
XP_005248351.1:n.2478+191C>T
|
|
XM_011514033.3:c.2682+191C>T
|
XP_011512335.1:n.2682+191C>T
|
|
XM_017009399.2:c.2565+191C>T
|
XP_016864888.1:n.2565+191C>T
|
|
XM_017009400.2:c.2547+191C>T
|
XP_016864889.1:n.2547+191C>T
|
|
XM_017009401.2:c.2454+191C>T
|
XP_016864890.1:n.2454+191C>T
|
|
XM_017009402.1:c.978+191C>T
|
XP_016864891.1:n.978+191C>T
|
|
XM_024446033.1:c.2682+191C>T
|
XP_024301801.1:n.2682+191C>T
|
|
XM_024446034.1:c.2682+191C>T
|
XP_024301802.1:n.2682+191C>T
|
|
XM_024446035.1:c.2571+191C>T
|
XP_024301803.1:n.2571+191C>T
|
|
XM_024446036.1:c.2682+191C>T
|
XP_024301804.1:n.2682+191C>T
|
|
NM_001100412.2:c.2571+191C>T
|
NP_001093882.1:n.2571+191C>T
|
|
NM_013235.5:c.2682+191C>T
|
NP_037367.3:n.2682+191C>T
|
|
NM_001382508.1:c.2682+191C>T
MANE Select
|
NP_001369437.1:n.2682+191C>T
|
|