|
ENST00000700029.2:c.736_738delinsGGT
|
ENSP00000514759.2:p.Pro246Gly
|
|
|
ENST00000710265.1:c.736_738delinsGGT
|
ENSP00000518161.1:p.Pro246Gly
|
|
|
ENST00000472832.3:c.736_738delinsGGT
|
ENSP00000483066.2:p.Pro246Gly
|
|
|
ENST00000688158.2:n.1471_1473delinsGGT
|
|
|
|
ENST00000688922.2:c.*566_*568delinsGGT
|
ENSP00000508742.2:n.*566_*568delinsGGT
|
|
|
ENST00000700021.1:c.691_693delinsGGT
|
ENSP00000514757.1:p.Pro231Gly
|
|
|
ENST00000700022.1:c.*75_*77delinsGGT
|
ENSP00000514758.1:n.*75_*77delinsGGT
|
|
|
ENST00000700023.1:n.1894_1896delinsGGT
|
|
|
|
ENST00000700024.1:n.2128_2130delinsGGT
|
|
|
|
ENST00000700025.1:n.1505_1507delinsGGT
|
|
|
|
ENST00000700026.1:n.373_375delinsGGT
|
|
|
|
ENST00000700029.1:c.570_572delinsGGT
|
|
|
|
ENST00000706954.1:c.736_738delinsGGT
|
ENSP00000516674.1:p.Pro246Gly
|
|
|
ENST00000706955.1:c.*771_*773delinsGGT
|
ENSP00000516675.1:n.*771_*773delinsGGT
|
|
|
ENST00000686459.1:c.*322_*324delinsGGT
|
ENSP00000508909.1:n.*322_*324delinsGGT
|
|
|
ENST00000688158.1:c.*847_*849delinsGGT
|
ENSP00000509254.1:n.*847_*849delinsGGT
|
|
|
ENST00000688308.1:c.736_738delinsGGT
|
ENSP00000508752.1:p.Pro246Gly
|
|
|
ENST00000688922.1:c.657_659delinsGGT
|
|
|
|
ENST00000693560.1:c.1255_1257delinsGGT
|
ENSP00000509861.1:p.Pro419Gly
|
|
|
ENST00000371953.8:c.736_738delinsGGT
MANE Select
|
ENSP00000361021.3:p.Pro246Gly
|
|
|
ENST00000371953.7:c.736_738delinsGGT
|
ENSP00000361021.3:p.Pro246Gly
|
|
|
ENST00000472832.2:c.163_165delinsGGT
|
ENSP00000483066.1:p.Pro55Gly
|
|
|
NM_000314.5:c.736_738delinsGGT
|
NP_000305.3:p.Pro246Gly
|
|
|
NM_000314.6:c.736_738delinsGGT
|
NP_000305.3:p.Pro246Gly
|
|
|
NM_001304717.2:c.1255_1257delinsGGT
|
NP_001291646.2:p.Pro419Gly
|
|
|
NM_001304718.1:c.145_147delinsGGT
|
NP_001291647.1:p.Pro49Gly
|
|
|
XM_006717926.2:c.691_693delinsGGT
|
XP_006717989.1:p.Pro231Gly
|
|
|
XM_011539981.1:c.736_738delinsGGT
|
XP_011538283.1:p.Pro246Gly
|
|
|
XM_011539982.1:c.640_642delinsGGT
|
XP_011538284.1:p.Pro214Gly
|
|
|
XR_945791.1:n.1306_1308delinsGGT
|
|
|
|
NM_000314.7:c.736_738delinsGGT
|
NP_000305.3:p.Pro246Gly
|
|
|
NM_001304717.5:c.1255_1257delinsGGT
|
NP_001291646.4:p.Pro419Gly
|
|
|
NM_001304718.2:c.145_147delinsGGT
|
NP_001291647.1:p.Pro49Gly
|
|
|
NM_000314.8:c.736_738delinsGGT
MANE Select
|
NP_000305.3:p.Pro246Gly
|
|
