ENST00000354393.7:c.2565T>G
|
ENSP00000346369.2:p.Ser855=
|
|
ENST00000540630.6:c.3444T>G
|
ENSP00000441668.3:p.Ser1148=
|
|
ENST00000613327.5:c.3390T>G
|
ENSP00000480757.2:p.Ser1130=
|
|
ENST00000688812.1:c.*653T>G
|
ENSP00000510658.1:n.*653T>G
|
|
ENST00000690544.1:c.*2661T>G
|
ENSP00000508989.1:n.*2661T>G
|
|
ENST00000358913.10:c.3390T>G
MANE Select
|
ENSP00000351790.5:p.Ser1130=
|
|
ENST00000354393.6:c.2565T>G
|
ENSP00000346369.2:p.Ser855=
|
|
ENST00000358913.9:c.3390T>G
|
ENSP00000351790.5:p.Ser1130=
|
|
ENST00000540630.5:c.3390T>G
|
ENSP00000441668.2:p.Ser1130=
|
|
ENST00000613327.4:c.2508T>G
|
ENSP00000480757.1:p.Ser836=
|
|
NM_001256267.1:c.3390T>G
|
NP_001243196.1:p.Ser1130=
|
|
NM_001256268.1:c.2508T>G
|
NP_001243197.1:p.Ser836=
|
|
NM_032578.3:c.3390T>G , LRG_410t1:c.3390T>G
|
NP_115967.2:p.Ser1130=
|
|
NR_045662.3:n.2817T>G
|
|
|
NR_045663.3:n.3519T>G
|
|
|
XM_006718043.2:c.3444T>G
|
XP_006718106.1:p.Ser1148=
|
|
XM_011540292.1:c.3420T>G
|
XP_011538594.1:p.Ser1140=
|
|
XR_946029.1:n.1804-197A>C
|
|
|
XM_017016833.1:c.3468T>G
|
XP_016872322.1:p.Ser1156=
|
|
XM_017016834.2:c.3390T>G
|
XP_016872323.1:p.Ser1130=
|
|
XM_024448236.1:c.2268T>G
|
XP_024304004.1:p.Ser756=
|
|
NR_045662.4:n.2927T>G
|
|
|
NR_045663.4:n.3464T>G
|
|
|
NM_001256267.2:c.3390T>G
|
NP_001243196.1:p.Ser1130=
|
|
NM_001256268.2:c.2508T>G
|
NP_001243197.1:p.Ser836=
|
|
NM_032578.4:c.3390T>G
MANE Select
|
NP_115967.2:p.Ser1130=
|
|