|
ENST00000713579.1:c.*77G>A
|
ENSP00000518871.1:n.*77G>A
|
|
|
ENST00000368797.10:c.*77G>A
MANE Select
|
ENSP00000357787.4:n.*77G>A
|
|
|
ENST00000465577.6:c.895G>A
|
|
|
|
ENST00000648427.1:c.*873G>A
|
ENSP00000497909.1:n.*873G>A
|
|
|
ENST00000649536.1:c.*77G>A
|
ENSP00000497817.1:n.*77G>A
|
|
|
ENST00000650472.1:n.3261G>A
|
|
|
|
ENST00000650524.1:c.788G>A
|
ENSP00000498108.1:n.788G>A
|
|
|
ENST00000650587.1:c.*77G>A
|
ENSP00000497366.1:n.*77G>A
|
|
|
ENST00000368786.5:c.*77G>A
|
ENSP00000357775.1:n.*77G>A
|
|
|
ENST00000368797.8:c.*77G>A
|
ENSP00000357787.4:n.*77G>A
|
|
|
ENST00000464267.1:n.972G>A
|
|
|
|
ENST00000465577.5:n.517G>A
|
|
|
|
ENST00000470483.1:n.563G>A
|
|
|
|
ENST00000484541.5:n.648G>A
|
|
|
|
ENST00000616800.4:c.161-3531G>A
|
|
|
|
ENST00000622016.4:c.241-2952G>A
|
ENSP00000483041.1:n.241-2952G>A
|
|
|
NM_000375.2:c.*77G>A
|
NP_000366.1:n.*77G>A
|
|
|
XM_005270137.2:c.*77G>A
|
XP_005270194.1:n.*77G>A
|
|
|
XM_005270138.2:c.*77G>A
|
XP_005270195.1:n.*77G>A
|
|
|
XM_005270139.2:c.661-2952G>A
|
XP_005270196.1:n.661-2952G>A
|
|
|
XM_006717960.2:c.*77G>A
|
XP_006718023.1:n.*77G>A
|
|
|
XM_011540127.1:c.661-3531G>A
|
XP_011538429.1:n.661-3531G>A
|
|
|
XR_246103.2:n.1055G>A
|
|
|
|
XR_945810.1:n.1285G>A
|
|
|
|
NM_000375.3:c.*77G>A
MANE Select
|
NP_000366.1:n.*77G>A
|
|
|
NM_001324036.1:c.*77G>A
|
NP_001310965.1:n.*77G>A
|
|
|
NM_001324037.1:c.*77G>A
|
NP_001310966.1:n.*77G>A
|
|
|
NM_001324038.1:c.*77G>A
|
NP_001310967.1:n.*77G>A
|
|
|
NR_136675.1:n.960G>A
|
|
|
|
NR_136676.1:n.1387G>A
|
|
|
|
NR_136677.1:n.927-2952G>A
|
|
|
|
NR_136678.1:n.871G>A
|
|
|
|
XM_011540127.2:c.661-3531G>A
|
XP_011538429.1:n.661-3531G>A
|
|
|
XM_017016611.2:c.*77G>A
|
XP_016872100.2:n.*77G>A
|
|
|
XM_017016612.2:c.661-2952G>A
|
XP_016872101.1:n.661-2952G>A
|
|
|
XM_024448154.1:c.*77G>A
|
XP_024303922.1:n.*77G>A
|
|
|
XR_002957010.1:n.2214G>A
|
|
|
|
XR_246103.3:n.1070G>A
|
|
|
|
XR_945810.2:n.1300G>A
|
|
|
|
NM_001324036.2:c.*77G>A
|
NP_001310965.1:n.*77G>A
|
|
|
NM_001324037.2:c.*77G>A
|
NP_001310966.1:n.*77G>A
|
|
|
NM_001324038.2:c.*77G>A
|
NP_001310967.1:n.*77G>A
|
|
|
NR_136675.2:n.950G>A
|
|
|
|
NR_136676.2:n.1377G>A
|
|
|
|
NR_136678.2:n.861G>A
|
|
|
|
NR_136677.2:n.917-2952G>A
|
|
|
