ENST00000354393.7:c.2701G>T
|
ENSP00000346369.2:p.Glu901Ter
|
|
ENST00000540630.6:c.3580G>T
|
ENSP00000441668.3:p.Glu1194Ter
|
|
ENST00000613327.5:c.3526G>T
|
ENSP00000480757.2:p.Glu1176Ter
|
|
ENST00000688812.1:c.*789G>T
|
ENSP00000510658.1:n.*789G>T
|
|
ENST00000690544.1:c.*2797G>T
|
ENSP00000508989.1:n.*2797G>T
|
|
ENST00000358913.10:c.3526G>T
MANE Select
|
ENSP00000351790.5:p.Glu1176Ter
|
|
ENST00000354393.6:c.2701G>T
|
ENSP00000346369.2:p.Glu901Ter
|
|
ENST00000358913.9:c.3526G>T
|
ENSP00000351790.5:p.Glu1176Ter
|
|
ENST00000540630.5:c.3526G>T
|
ENSP00000441668.2:p.Glu1176Ter
|
|
ENST00000613327.4:c.2644G>T
|
ENSP00000480757.1:p.Glu882Ter
|
|
NM_001256267.1:c.3526G>T
|
NP_001243196.1:p.Glu1176Ter
|
|
NM_001256268.1:c.2644G>T
|
NP_001243197.1:p.Glu882Ter
|
|
NM_032578.3:c.3526G>T , LRG_410t1:c.3526G>T
|
NP_115967.2:p.Glu1176Ter
|
|
NR_045662.3:n.2953G>T
|
|
|
NR_045663.3:n.3655G>T
|
|
|
XM_006718043.2:c.3580G>T
|
XP_006718106.1:p.Glu1194Ter
|
|
XM_011540292.1:c.3556G>T
|
XP_011538594.1:p.Glu1186Ter
|
|
XR_946029.1:n.1803+2170C>A
|
|
|
XM_017016833.1:c.3604G>T
|
XP_016872322.1:p.Glu1202Ter
|
|
XM_017016834.2:c.3526G>T
|
XP_016872323.1:p.Glu1176Ter
|
|
XM_024448236.1:c.2404G>T
|
XP_024304004.1:p.Glu802Ter
|
|
NR_045662.4:n.3063G>T
|
|
|
NR_045663.4:n.3600G>T
|
|
|
NM_001256267.2:c.3526G>T
|
NP_001243196.1:p.Glu1176Ter
|
|
NM_001256268.2:c.2644G>T
|
NP_001243197.1:p.Glu882Ter
|
|
NM_032578.4:c.3526G>T
MANE Select
|
NP_115967.2:p.Glu1176Ter
|
|