ENST00000366779.6:c.*343G>A
|
ENSP00000355741.2:n.*343G>A
|
|
ENST00000366782.6:c.*343G>A
|
ENSP00000355746.2:n.*343G>A
|
|
ENST00000366783.8:c.*343G>A
MANE Select
|
ENSP00000355747.3:n.*343G>A
|
|
ENST00000471728.2:n.2328G>A
|
|
|
ENST00000524196.6:c.*343G>A
|
ENSP00000429036.2:n.*343G>A
|
|
ENST00000626989.3:c.*343G>A
|
ENSP00000486498.2:n.*343G>A
|
|
ENST00000676467.1:c.*1517G>A
|
ENSP00000504294.1:n.*1517G>A
|
|
ENST00000676747.1:c.1189-1798G>A
|
ENSP00000503244.1:n.1189-1798G>A
|
|
ENST00000676884.1:c.*343G>A
|
ENSP00000503200.1:n.*343G>A
|
|
ENST00000676888.1:c.*1031G>A
|
ENSP00000504483.1:n.*1031G>A
|
|
ENST00000676907.1:c.*1269G>A
|
ENSP00000504410.1:n.*1269G>A
|
|
ENST00000676945.1:c.1191+1797G>A
|
ENSP00000504433.1:n.1191+1797G>A
|
|
ENST00000677065.1:n.2251G>A
|
|
|
ENST00000677414.1:c.*343G>A
|
ENSP00000503116.1:n.*343G>A
|
|
ENST00000677529.1:n.3420G>A
|
|
|
ENST00000677596.1:c.*1912G>A
|
ENSP00000503618.1:n.*1912G>A
|
|
ENST00000677599.1:c.1191+1797G>A
|
ENSP00000503673.1:n.1191+1797G>A
|
|
ENST00000677748.1:n.3945G>A
|
|
|
ENST00000677880.1:c.*343G>A
|
ENSP00000503121.1:n.*343G>A
|
|
ENST00000678021.1:c.*1313G>A
|
ENSP00000504674.1:n.*1313G>A
|
|
ENST00000678233.1:c.*8+335G>A
|
ENSP00000504728.1:n.*8+335G>A
|
|
ENST00000678320.1:c.*343G>A
|
ENSP00000503680.1:n.*343G>A
|
|
ENST00000678655.1:c.1093-1798G>A
|
ENSP00000504230.1:n.1093-1798G>A
|
|
ENST00000678706.1:c.*1067G>A
|
ENSP00000503659.1:n.*1067G>A
|
|
ENST00000678776.1:c.*1827G>A
|
ENSP00000504624.1:n.*1827G>A
|
|
ENST00000678784.1:c.1073-1798G>A
|
ENSP00000504652.1:n.1073-1798G>A
|
|
ENST00000678820.1:c.1090-1798G>A
|
ENSP00000504138.1:n.1090-1798G>A
|
|
ENST00000678835.1:c.*757-1798G>A
|
ENSP00000504343.1:n.*757-1798G>A
|
|
ENST00000679088.1:c.*343G>A
|
ENSP00000504727.1:n.*343G>A
|
|
ENST00000679098.1:c.*8+335G>A
|
ENSP00000504303.1:n.*8+335G>A
|
|
ENST00000366782.5:c.*343G>A
|
ENSP00000355746.1:n.*343G>A
|
|
ENST00000366783.7:c.*343G>A
|
ENSP00000355747.3:n.*343G>A
|
|
ENST00000626989.2:c.1789G>A
|
ENSP00000486498.1:n.1789G>A
|
|
NM_000447.2:c.*343G>A
|
NP_000438.2:n.*343G>A
|
|
NM_012486.2:c.*343G>A
|
NP_036618.2:n.*343G>A
|
|
XM_005273199.2:c.*343G>A
|
XP_005273256.1:n.*343G>A
|
|
XM_011544236.1:c.*343G>A
|
XP_011542538.1:n.*343G>A
|
|
XM_005273199.4:c.*343G>A
|
XP_005273256.1:n.*343G>A
|
|
XM_017001835.1:c.*343G>A
|
XP_016857324.1:n.*343G>A
|
|
XM_017001836.1:c.*343G>A
|
XP_016857325.1:n.*343G>A
|
|
XR_001737316.2:n.1478-1798G>A
|
|
|
XR_001737317.2:n.1478-1798G>A
|
|
|
XR_001737318.2:n.2405G>A
|
|
|
XR_001737319.1:n.2748G>A
|
|
|
XR_001737320.1:n.2745G>A
|
|
|
XR_001737321.1:n.2240G>A
|
|
|
XR_949149.2:n.2402G>A
|
|
|
XR_949150.3:n.2621G>A
|
|
|
NM_000447.3:c.*343G>A
MANE Select
|
NP_000438.2:n.*343G>A
|
|
NM_012486.3:c.*343G>A
|
NP_036618.2:n.*343G>A
|
|