ENST00000391944.8:c.2171T>C
|
ENSP00000375808.4:p.Met724Thr
|
|
ENST00000682414.1:c.2171T>C
|
ENSP00000507019.1:p.Met724Thr
|
|
ENST00000682508.1:n.2200T>C
|
|
|
ENST00000684218.1:c.*1429T>C
|
ENSP00000507804.1:n.*1429T>C
|
|
ENST00000684264.1:n.1727T>C
|
|
|
ENST00000684407.1:c.2048T>C
|
ENSP00000507775.1:p.Met683Thr
|
|
ENST00000684458.1:c.*657T>C
|
ENSP00000508260.1:n.*657T>C
|
|
ENST00000684468.1:n.1883T>C
|
|
|
ENST00000391945.10:c.2171T>C
MANE Select
|
ENSP00000375809.4:p.Met724Thr
|
|
ENST00000646507.1:n.2268T>C
|
|
|
ENST00000391941.6:c.2099T>C
|
ENSP00000375805.2:p.Met700Thr
|
|
ENST00000391942.6:n.1342T>C
|
|
|
ENST00000391944.7:c.1937T>C
|
ENSP00000375808.3:p.Met646Thr
|
|
ENST00000391945.8:c.2171T>C
|
ENSP00000375809.3:p.Met724Thr
|
|
ENST00000588652.5:n.2259T>C
|
|
|
NM_000400.3:c.2171T>C , LRG_461t1:c.2171T>C
|
NP_000391.1:p.Met724Thr
|
|
XM_011526611.1:c.2093T>C
|
XP_011524913.1:p.Met698Thr
|
|
XM_011526611.2:c.2093T>C
|
XP_011524913.1:p.Met698Thr
|
|
XM_017026467.1:c.2048T>C
|
XP_016881956.1:p.Met683Thr
|
|
XR_001753633.2:n.2218T>C
|
|
|
XR_001753634.2:n.2154T>C
|
|
|
NM_000400.4:c.2171T>C
MANE Select
|
NP_000391.1:p.Met724Thr
|
|