ENST00000320005.6:c.428_446delinsCAGCCCTCTACAAGAAAAA
MANE Select
|
ENSP00000316605.5:p.Thr143=
|
|
ENST00000680314.1:n.189_207delinsCAGCCCTCTACAAGAAAAA
|
|
|
ENST00000681746.1:c.428_446delinsCAGCCCTCTACAAGAAAAA
|
ENSP00000505959.1:p.Thr143=
|
|
ENST00000320005.5:c.428_446delinsCAGCCCTCTACAAGAAAAA
|
ENSP00000316605.5:p.Thr143=
|
|
NM_019098.4:c.428_446delinsCAGCCCTCTACAAGAAAAA
|
NP_061971.3:p.Thr143=
|
|
XM_011517138.1:c.14_32delinsCAGCCCTCTACAAGAAAAA
|
XP_011515440.1:p.Thr5=
|
|
XM_011517138.2:c.14_32delinsCAGCCCTCTACAAGAAAAA
|
XP_011515440.1:p.Thr5=
|
|
NM_019098.5:c.428_446delinsCAGCCCTCTACAAGAAAAA
MANE Select
|
NP_061971.3:p.Thr143=
|
|