|
ENST00000366779.6:c.*435A>G
|
ENSP00000355741.2:n.*435A>G
|
|
|
ENST00000366782.6:c.*435A>G
|
ENSP00000355746.2:n.*435A>G
|
|
|
ENST00000366783.8:c.*435A>G
MANE Select
|
ENSP00000355747.3:n.*435A>G
|
|
|
ENST00000471728.2:n.2420A>G
|
|
|
|
ENST00000524196.6:c.*435A>G
|
ENSP00000429036.2:n.*435A>G
|
|
|
ENST00000626989.3:c.*435A>G
|
ENSP00000486498.2:n.*435A>G
|
|
|
ENST00000676467.1:c.*1609A>G
|
ENSP00000504294.1:n.*1609A>G
|
|
|
ENST00000676747.1:c.1189-1706A>G
|
ENSP00000503244.1:n.1189-1706A>G
|
|
|
ENST00000676884.1:c.*435A>G
|
ENSP00000503200.1:n.*435A>G
|
|
|
ENST00000676888.1:c.*1123A>G
|
ENSP00000504483.1:n.*1123A>G
|
|
|
ENST00000676907.1:c.*1361A>G
|
ENSP00000504410.1:n.*1361A>G
|
|
|
ENST00000676945.1:c.1191+1889A>G
|
ENSP00000504433.1:n.1191+1889A>G
|
|
|
ENST00000677065.1:n.2343A>G
|
|
|
|
ENST00000677414.1:c.*435A>G
|
ENSP00000503116.1:n.*435A>G
|
|
|
ENST00000677529.1:n.3512A>G
|
|
|
|
ENST00000677596.1:c.*2004A>G
|
ENSP00000503618.1:n.*2004A>G
|
|
|
ENST00000677599.1:c.1191+1889A>G
|
ENSP00000503673.1:n.1191+1889A>G
|
|
|
ENST00000677748.1:n.4037A>G
|
|
|
|
ENST00000677880.1:c.*435A>G
|
ENSP00000503121.1:n.*435A>G
|
|
|
ENST00000678021.1:c.*1405A>G
|
ENSP00000504674.1:n.*1405A>G
|
|
|
ENST00000678233.1:c.*8+427A>G
|
ENSP00000504728.1:n.*8+427A>G
|
|
|
ENST00000678320.1:c.*435A>G
|
ENSP00000503680.1:n.*435A>G
|
|
|
ENST00000678655.1:c.1093-1706A>G
|
ENSP00000504230.1:n.1093-1706A>G
|
|
|
ENST00000678706.1:c.*1159A>G
|
ENSP00000503659.1:n.*1159A>G
|
|
|
ENST00000678776.1:c.*1919A>G
|
ENSP00000504624.1:n.*1919A>G
|
|
|
ENST00000678784.1:c.1073-1706A>G
|
ENSP00000504652.1:n.1073-1706A>G
|
|
|
ENST00000678820.1:c.1090-1706A>G
|
ENSP00000504138.1:n.1090-1706A>G
|
|
|
ENST00000678835.1:c.*757-1706A>G
|
ENSP00000504343.1:n.*757-1706A>G
|
|
|
ENST00000679088.1:c.*435A>G
|
ENSP00000504727.1:n.*435A>G
|
|
|
ENST00000679098.1:c.*8+427A>G
|
ENSP00000504303.1:n.*8+427A>G
|
|
|
ENST00000366782.5:c.*435A>G
|
ENSP00000355746.1:n.*435A>G
|
|
|
ENST00000366783.7:c.*435A>G
|
ENSP00000355747.3:n.*435A>G
|
|
|
ENST00000626989.2:c.1881A>G
|
ENSP00000486498.1:n.1881A>G
|
|
|
NM_000447.2:c.*435A>G
|
NP_000438.2:n.*435A>G
|
|
|
NM_012486.2:c.*435A>G
|
NP_036618.2:n.*435A>G
|
|
|
XM_005273199.2:c.*435A>G
|
XP_005273256.1:n.*435A>G
|
|
|
XM_011544236.1:c.*435A>G
|
XP_011542538.1:n.*435A>G
|
|
|
XM_005273199.4:c.*435A>G
|
XP_005273256.1:n.*435A>G
|
|
|
XM_017001835.1:c.*435A>G
|
XP_016857324.1:n.*435A>G
|
|
|
XM_017001836.1:c.*435A>G
|
XP_016857325.1:n.*435A>G
|
|
|
XR_001737316.2:n.1478-1706A>G
|
|
|
|
XR_001737317.2:n.1478-1706A>G
|
|
|
|
XR_001737318.2:n.2497A>G
|
|
|
|
XR_001737319.1:n.2840A>G
|
|
|
|
XR_001737320.1:n.2837A>G
|
|
|
|
XR_001737321.1:n.2332A>G
|
|
|
|
XR_949149.2:n.2494A>G
|
|
|
|
XR_949150.3:n.2713A>G
|
|
|
|
NM_000447.3:c.*435A>G
MANE Select
|
NP_000438.2:n.*435A>G
|
|
|
NM_012486.3:c.*435A>G
|
NP_036618.2:n.*435A>G
|
|
