ENST00000354393.7:c.2323C>T
|
ENSP00000346369.2:p.Gln775Ter
|
|
ENST00000540630.6:c.3202C>T
|
ENSP00000441668.3:p.Gln1068Ter
|
|
ENST00000613327.5:c.3148C>T
|
ENSP00000480757.2:p.Gln1050Ter
|
|
ENST00000688812.1:c.*411C>T
|
ENSP00000510658.1:n.*411C>T
|
|
ENST00000690544.1:c.*2419C>T
|
ENSP00000508989.1:n.*2419C>T
|
|
ENST00000358913.10:c.3148C>T
MANE Select
|
ENSP00000351790.5:p.Gln1050Ter
|
|
ENST00000354393.6:c.2323C>T
|
ENSP00000346369.2:p.Gln775Ter
|
|
ENST00000358913.9:c.3148C>T
|
ENSP00000351790.5:p.Gln1050Ter
|
|
ENST00000540630.5:c.3148C>T
|
ENSP00000441668.2:p.Gln1050Ter
|
|
ENST00000613327.4:c.2266C>T
|
ENSP00000480757.1:p.Gln756Ter
|
|
NM_001256267.1:c.3148C>T
|
NP_001243196.1:p.Gln1050Ter
|
|
NM_001256268.1:c.2266C>T
|
NP_001243197.1:p.Gln756Ter
|
|
NM_032578.3:c.3148C>T , LRG_410t1:c.3148C>T
|
NP_115967.2:p.Gln1050Ter
|
|
NR_045662.3:n.2575C>T
|
|
|
NR_045663.3:n.3277C>T
|
|
|
XM_006718043.2:c.3202C>T
|
XP_006718106.1:p.Gln1068Ter
|
|
XM_011540292.1:c.3178C>T
|
XP_011538594.1:p.Gln1060Ter
|
|
XM_017016833.1:c.3226C>T
|
XP_016872322.1:p.Gln1076Ter
|
|
XM_017016834.2:c.3148C>T
|
XP_016872323.1:p.Gln1050Ter
|
|
XM_024448236.1:c.2026C>T
|
XP_024304004.1:p.Gln676Ter
|
|
NR_045662.4:n.2685C>T
|
|
|
NR_045663.4:n.3222C>T
|
|
|
NM_001256267.2:c.3148C>T
|
NP_001243196.1:p.Gln1050Ter
|
|
NM_001256268.2:c.2266C>T
|
NP_001243197.1:p.Gln756Ter
|
|
NM_032578.4:c.3148C>T
MANE Select
|
NP_115967.2:p.Gln1050Ter
|
|