ENST00000354393.7:c.*112G>T
|
ENSP00000346369.2:n.*112G>T
|
|
ENST00000540630.6:c.*112G>T
|
ENSP00000441668.3:n.*112G>T
|
|
ENST00000613327.5:c.*112G>T
|
ENSP00000480757.2:n.*112G>T
|
|
ENST00000688812.1:c.*1338G>T
|
ENSP00000510658.1:n.*1338G>T
|
|
ENST00000690544.1:c.*3346G>T
|
ENSP00000508989.1:n.*3346G>T
|
|
ENST00000358913.10:c.*112G>T
MANE Select
|
ENSP00000351790.5:n.*112G>T
|
|
ENST00000354393.6:c.*112G>T
|
ENSP00000346369.2:n.*112G>T
|
|
ENST00000358913.9:c.*112G>T
|
ENSP00000351790.5:n.*112G>T
|
|
ENST00000540630.5:c.*112G>T
|
ENSP00000441668.2:n.*112G>T
|
|
ENST00000613327.4:c.*112G>T
|
ENSP00000480757.1:n.*112G>T
|
|
NM_001256267.1:c.*112G>T
|
NP_001243196.1:n.*112G>T
|
|
NM_001256268.1:c.*112G>T
|
NP_001243197.1:n.*112G>T
|
|
NM_032578.3:c.*112G>T , LRG_410t1:c.*112G>T
|
NP_115967.2:n.*112G>T
|
|
NR_045662.3:n.3502G>T
|
|
|
NR_045663.3:n.4204G>T
|
|
|
XM_006718043.2:c.*112G>T
|
XP_006718106.1:n.*112G>T
|
|
XM_011540292.1:c.*112G>T
|
XP_011538594.1:n.*112G>T
|
|
XR_946029.1:n.1574+4721C>A
|
|
|
XM_017016833.1:c.*112G>T
|
XP_016872322.1:n.*112G>T
|
|
XM_017016834.2:c.*112G>T
|
XP_016872323.1:n.*112G>T
|
|
XM_024448236.1:c.*112G>T
|
XP_024304004.1:n.*112G>T
|
|
NR_045662.4:n.3612G>T
|
|
|
NR_045663.4:n.4149G>T
|
|
|
NM_001256267.2:c.*112G>T
|
NP_001243196.1:n.*112G>T
|
|
NM_001256268.2:c.*112G>T
|
NP_001243197.1:n.*112G>T
|
|
NM_032578.4:c.*112G>T
MANE Select
|
NP_115967.2:n.*112G>T
|
|