ENST00000403665.7:c.1163T>A
MANE Select
|
ENSP00000384957.2:p.Ile388Asn
|
|
ENST00000264692.8:c.1001T>A
|
ENSP00000264692.5:p.Ile334Asn
|
|
ENST00000403665.6:c.1163T>A
|
ENSP00000384957.2:p.Ile388Asn
|
|
NM_000128.3:c.1163T>A , LRG_583t1:c.1163T>A
|
NP_000119.1:p.Ile388Asn
|
|
XM_005262821.2:c.1166T>A
|
XP_005262878.1:p.Ile389Asn
|
|
XM_005262822.2:c.1166T>A
|
XP_005262879.1:p.Ile389Asn
|
|
XM_005262823.2:c.896T>A
|
XP_005262880.1:p.Ile299Asn
|
|
XM_005262824.1:c.1166T>A
|
XP_005262881.1:p.Ile389Asn
|
|
XM_006714137.1:c.1118T>A
|
XP_006714200.1:p.Ile373Asn
|
|
XR_938706.1:n.1571T>A
|
|
|
XR_938707.1:n.1571T>A
|
|
|
XM_005262821.4:c.1166T>A
|
XP_005262878.1:p.Ile389Asn
|
|
XM_005262822.4:c.1166T>A
|
XP_005262879.1:p.Ile389Asn
|
|
XM_005262823.4:c.896T>A
|
XP_005262880.1:p.Ile299Asn
|
|
XM_006714137.3:c.1118T>A
|
XP_006714200.1:p.Ile373Asn
|
|
XM_017007884.2:c.*2135T>A
|
XP_016863373.1:n.*2135T>A
|
|
XM_017007885.2:c.*31T>A
|
XP_016863374.1:n.*31T>A
|
|
XR_001741172.2:n.1637T>A
|
|
|
NM_000128.4:c.1163T>A
MANE Select
|
NP_000119.1:p.Ile388Asn
|
|