ENST00000324862.7:c.1793T>C
MANE Select
|
ENSP00000315379.6:p.Met598Thr
|
|
ENST00000324862.6:c.1793T>C
|
ENSP00000315379.6:p.Met598Thr
|
|
ENST00000467329.5:n.2120T>C
|
|
|
ENST00000476970.1:n.902T>C
|
|
|
NM_004698.2:c.1793T>C
|
NP_004689.1:p.Met598Thr
|
|
XM_011510128.1:c.1793T>C
|
XP_011508430.1:p.Met598Thr
|
|
XM_011510129.1:c.1388T>C
|
XP_011508431.1:p.Met463Thr
|
|
XM_011510130.1:c.1361T>C
|
XP_011508432.1:p.Met454Thr
|
|
XR_241103.1:n.1776T>C
|
|
|
XR_921997.1:n.1776T>C
|
|
|
XR_921998.1:n.1890T>C
|
|
|
NM_001350529.1:c.1388T>C
|
NP_001337458.1:p.Met463Thr
|
|
NM_004698.3:c.1793T>C
|
NP_004689.1:p.Met598Thr
|
|
NR_146766.1:n.2024T>C
|
|
|
NR_146767.1:n.2120T>C
|
|
|
NR_146768.1:n.1966T>C
|
|
|
NR_146769.1:n.2019T>C
|
|
|
XM_011510130.3:c.1361T>C
|
XP_011508432.1:p.Met454Thr
|
|
XM_017002790.1:c.1361T>C
|
XP_016858279.1:p.Met454Thr
|
|
XR_001737536.2:n.1826T>C
|
|
|
XR_001737537.2:n.1940T>C
|
|
|
XR_001737540.2:n.2697T>C
|
|
|
XR_001737541.2:n.1720T>C
|
|
|
XR_002958009.1:n.2450T>C
|
|
|
XR_002958010.1:n.3686T>C
|
|
|
XR_002958012.1:n.1882T>C
|
|
|
XR_241103.3:n.1768T>C
|
|
|
XR_921997.3:n.1768T>C
|
|
|
XR_921998.3:n.1882T>C
|
|
|
NM_004698.4:c.1793T>C
MANE Select
|
NP_004689.1:p.Met598Thr
|
|