|
ENST00000356839.10:c.1187T>C
MANE Select
|
ENSP00000349297.5:p.Met396Thr
|
|
|
ENST00000322910.9:c.*1142T>C
|
ENSP00000325395.5:n.*1142T>C
|
|
|
ENST00000350303.9:c.1121T>C
|
ENSP00000344152.5:p.Met374Thr
|
|
|
ENST00000356839.9:c.1187T>C
|
ENSP00000349297.5:p.Met396Thr
|
|
|
ENST00000542255.6:c.45T>C
|
|
|
|
ENST00000543245.6:c.1256T>C
|
ENSP00000438689.2:p.Met419Thr
|
|
|
ENST00000578579.2:n.358T>C
|
|
|
|
ENST00000578711.1:n.144T>C
|
|
|
|
ENST00000578824.5:n.603T>C
|
|
|
|
ENST00000579425.5:n.211T>C
|
|
|
|
ENST00000579546.1:c.24T>C
|
|
|
|
ENST00000583858.5:c.216T>C
|
|
|
|
ENST00000585203.6:n.395T>C
|
|
|
|
NM_000018.3:c.1187T>C
|
NP_000009.1:p.Met396Thr
|
|
|
NM_001033859.2:c.1121T>C
|
NP_001029031.1:p.Met374Thr
|
|
|
NM_001270447.1:c.1256T>C
|
NP_001257376.1:p.Met419Thr
|
|
|
NM_001270448.1:c.959T>C
|
NP_001257377.1:p.Met320Thr
|
|
|
XM_006721516.2:c.1187T>C
|
XP_006721579.2:p.Met396Thr
|
|
|
XM_011523829.1:c.1187T>C
|
XP_011522131.1:p.Met396Thr
|
|
|
XM_011523830.1:c.1187T>C
|
XP_011522132.1:p.Met396Thr
|
|
|
XR_934021.1:n.1294T>C
|
|
|
|
XR_934022.1:n.1294T>C
|
|
|
|
XR_934023.1:n.1294T>C
|
|
|
|
XM_006721516.3:c.1187T>C
|
XP_006721579.2:p.Met396Thr
|
|
|
XM_011523829.2:c.1187T>C
|
XP_011522131.1:p.Met396Thr
|
|
|
XM_011523830.2:c.1187T>C
|
XP_011522132.1:p.Met396Thr
|
|
|
XM_024450741.1:c.1187T>C
|
XP_024306509.1:p.Met396Thr
|
|
|
XR_934021.2:n.1246T>C
|
|
|
|
XR_934022.2:n.1246T>C
|
|
|
|
XR_934023.2:n.1246T>C
|
|
|
|
NM_000018.4:c.1187T>C
MANE Select
|
NP_000009.1:p.Met396Thr
|
|
|
NM_001033859.3:c.1121T>C
|
NP_001029031.1:p.Met374Thr
|
|
|
NM_001270447.2:c.1256T>C
|
NP_001257376.1:p.Met419Thr
|
|
|
NM_001270448.2:c.959T>C
|
NP_001257377.1:p.Met320Thr
|
|
