ENST00000338468.8:c.1264G>A
|
ENSP00000343589.4:n.1264G>A
|
|
ENST00000366894.6:c.1145G>A
|
ENSP00000355860.2:n.1145G>A
|
|
ENST00000366898.6:c.1386G>A
MANE Select
|
ENSP00000355865.1:p.Trp462Ter
|
|
ENST00000673871.1:c.1467G>A
|
|
|
ENST00000674006.1:n.771G>A
|
|
|
ENST00000674436.1:n.1022G>A
|
|
|
ENST00000338468.7:c.813G>A
|
ENSP00000343589.3:p.Trp271Ter
|
|
ENST00000366894.5:c.813G>A
|
ENSP00000355860.1:p.Trp271Ter
|
|
ENST00000366896.5:c.939G>A
|
ENSP00000355862.1:p.Trp313Ter
|
|
ENST00000366897.5:c.1302G>A
|
ENSP00000355863.1:p.Trp434Ter
|
|
ENST00000366898.5:c.1386G>A
|
ENSP00000355865.1:p.Trp462Ter
|
|
ENST00000479615.5:c.*162G>A
|
ENSP00000434414.1:n.*162G>A
|
|
ENST00000610470.4:c.519G>A
|
ENSP00000483773.1:p.Trp173Ter
|
|
NM_004562.2:c.1386G>A
|
NP_004553.2:p.Trp462Ter
|
|
NM_013987.2:c.1302G>A
|
NP_054642.2:p.Trp434Ter
|
|
NM_013988.2:c.939G>A
|
NP_054643.2:p.Trp313Ter
|
|
XM_011535863.1:c.1383G>A
|
XP_011534165.1:p.Trp461Ter
|
|
XM_017010908.1:c.1500G>A
|
XP_016866397.1:p.Trp500Ter
|
|
XM_017010909.2:c.1146G>A
|
XP_016866398.1:p.Trp382Ter
|
|
XM_024446449.1:c.1149G>A
|
XP_024302217.1:p.Trp383Ter
|
|
XR_001743443.2:n.1578G>A
|
|
|
NM_004562.3:c.1386G>A
MANE Select
|
NP_004553.2:p.Trp462Ter
|
|
NM_013987.3:c.1302G>A
|
NP_054642.2:p.Trp434Ter
|
|
NM_013988.3:c.939G>A
|
NP_054643.2:p.Trp313Ter
|
|