ENST00000695844.1:n.1546G>A
|
|
|
ENST00000695845.1:n.1545G>A
|
|
|
ENST00000695846.1:n.1391G>A
|
|
|
ENST00000394634.7:c.1367G>A
MANE Select
|
ENSP00000378130.2:p.Trp456Ter
|
|
ENST00000394635.8:c.1391G>A
|
ENSP00000378131.3:p.Trp464Ter
|
|
ENST00000645635.1:c.1367G>A
|
ENSP00000493607.1:p.Trp456Ter
|
|
ENST00000394634.6:c.1367G>A
|
ENSP00000378130.2:p.Trp456Ter
|
|
ENST00000394635.7:c.1391G>A
|
ENSP00000378131.3:p.Trp464Ter
|
|
ENST00000504853.3:n.1784G>A
|
|
|
ENST00000512148.5:c.1346G>A
|
ENSP00000427438.1:p.Trp449Ter
|
|
ENST00000515512.1:n.9G>A
|
|
|
ENST00000618244.4:c.1044+3215G>A
|
ENSP00000483416.1:n.1044+3215G>A
|
|
NM_000204.3:c.1367G>A , LRG_48t1:c.1367G>A
|
NP_000195.2:p.Trp456Ter
|
|
XM_005262975.1:c.1391G>A
|
XP_005263032.1:p.Trp464Ter
|
|
XM_005262976.1:c.1346G>A
|
XP_005263033.1:p.Trp449Ter
|
|
XM_006714209.1:c.1388G>A
|
XP_006714272.1:p.Trp463Ter
|
|
XM_006714210.2:c.1391G>A
|
XP_006714273.1:p.Trp464Ter
|
|
XM_011531920.1:c.1391G>A
|
XP_011530222.1:p.Trp464Ter
|
|
NM_000204.4:c.1367G>A
|
NP_000195.2:p.Trp456Ter
|
|
NM_001318057.1:c.1391G>A
|
NP_001304986.1:p.Trp464Ter
|
|
NM_001331035.1:c.1346G>A
|
NP_001317964.1:p.Trp449Ter
|
|
XM_006714210.4:c.1391G>A
|
XP_006714273.1:p.Trp464Ter
|
|
XM_011531920.2:c.1391G>A
|
XP_011530222.1:p.Trp464Ter
|
|
XM_017008164.2:c.1367G>A
|
XP_016863653.1:p.Trp456Ter
|
|
XM_017008165.2:c.1346G>A
|
XP_016863654.1:p.Trp449Ter
|
|
XM_017008166.2:c.1367G>A
|
XP_016863655.1:p.Trp456Ter
|
|
NM_001318057.2:c.1391G>A
|
NP_001304986.2:p.Trp464Ter
|
|
NM_001331035.2:c.1346G>A
|
NP_001317964.1:p.Trp449Ter
|
|
NM_001375278.1:c.1391G>A
|
NP_001362207.1:p.Trp464Ter
|
|
NM_001375279.1:c.1367G>A
|
NP_001362208.1:p.Trp456Ter
|
|
NM_001375280.1:c.1346G>A
|
NP_001362209.1:p.Trp449Ter
|
|
NM_001375281.1:c.1367G>A
|
NP_001362210.1:p.Trp456Ter
|
|
NM_001375282.1:c.1346G>A
|
NP_001362211.1:p.Trp449Ter
|
|
NM_001375283.1:c.1310G>A
|
NP_001362212.1:p.Trp437Ter
|
|
NM_001375284.1:c.758G>A
|
NP_001362213.1:p.Trp253Ter
|
|
NR_164671.1:n.1176+2934G>A
|
|
|
NR_164672.1:n.1417G>A
|
|
|
NR_164673.1:n.1391G>A
|
|
|
NM_000204.5:c.1367G>A
MANE Select
|
NP_000195.3:p.Trp456Ter
|
|