|
NM_032119.4:c.17832G>T
MANE Select
|
NP_115495.3:p.Met5944Ile
|
|
ENST00000405460.9:c.17832G>T
MANE Select
|
ENSP00000384582.2:p.Met5944Ile
|
|
NM_032119.3:c.17832G>T
|
NP_115495.3:p.Met5944Ile
|
|
NR_003149.1:n.17845G>T
|
|
|
NR_003149.2:n.17848G>T
|
|
|
ENST00000405460.6:c.17832G>T
|
ENSP00000384582.2:p.Met5944Ile
|
|
ENST00000425867.2:c.4815G>T
|
ENSP00000392618.2:p.Met1605Ile
|
|
ENST00000425867.3:c.6786G>T
|
ENSP00000392618.3:p.Met2262Ile
|
|
ENST00000503852.1:n.380G>T
|
|
|
ENST00000638510.1:n.5099G>T
|
|
|
ENST00000638990.1:c.1044G>T
|
|
|
ENST00000639431.1:c.266-121511G>T
|
ENSP00000491057.1:n.266-121511G>T
|
|
ENST00000640407.1:c.4281G>T
|
ENSP00000491425.1:n.4281G>T
|
|
XM_011543675.1:c.17829G>T
|
XP_011541977.1:p.Met5943Ile
|
|
XM_011543676.1:c.17751G>T
|
XP_011541978.1:p.Met5917Ile
|
|
XM_011543677.1:c.15135G>T
|
XP_011541979.1:p.Met5045Ile
|
|
XM_017009963.2:c.17853G>T
|
XP_016865452.1:p.Met5951Ile
|
|
XM_017009964.2:c.17850G>T
|
XP_016865453.1:p.Met5950Ile
|
|
XM_017009965.1:c.17850G>T
|
XP_016865454.1:p.Met5950Ile
|
|
XM_017009966.2:c.17772G>T
|
XP_016865455.1:p.Met5924Ile
|
|
XM_017009967.1:c.17757G>T
|
XP_016865456.1:p.Met5919Ile
|
|
XM_017009968.2:c.17673G>T
|
XP_016865457.1:p.Met5891Ile
|
|
XM_017009969.2:c.17853G>T
|
XP_016865458.1:p.Met5951Ile
|
|
XM_017009972.1:c.10971G>T
|
XP_016865461.1:p.Met3657Ile
|
|
XM_017009973.1:c.10950G>T
|
XP_016865462.1:p.Met3650Ile
|