ENST00000298910.12:c.6079A>T
MANE Select
|
ENSP00000298910.7:p.Met2027Leu
|
|
ENST00000679360.1:c.*4988A>T
|
ENSP00000505368.1:n.*4988A>T
|
|
ENST00000679532.1:c.1853A>T
|
|
|
ENST00000680018.1:c.1524A>T
|
ENSP00000505347.1:n.1524A>T
|
|
ENST00000680422.1:c.1724A>T
|
|
|
ENST00000680425.1:c.1246A>T
|
ENSP00000506459.1:n.1246A>T
|
|
ENST00000680453.1:c.1536A>T
|
|
|
ENST00000680790.1:c.5824A>T
|
ENSP00000505335.1:p.Met1942Leu
|
|
ENST00000681136.1:n.2063A>T
|
|
|
ENST00000681696.1:c.1762A>T
|
ENSP00000505871.1:p.Met588Leu
|
|
ENST00000298910.11:c.6079A>T
|
ENSP00000298910.7:p.Met2027Leu
|
|
ENST00000430804.5:c.3375A>T
|
|
|
ENST00000479187.5:n.2760A>T
|
|
|
NM_198578.3:c.6079A>T
|
NP_940980.3:p.Met2027Leu
|
|
XM_005268629.2:c.6079A>T
|
XP_005268686.1:p.Met2027Leu
|
|
XM_011537877.1:c.6079A>T
|
XP_011536179.1:p.Met2027Leu
|
|
XM_011537878.1:c.6079A>T
|
XP_011536180.1:p.Met2027Leu
|
|
XM_011537879.1:c.4876A>T
|
XP_011536181.1:p.Met1626Leu
|
|
XM_005268629.4:c.6079A>T
|
XP_005268686.1:p.Met2027Leu
|
|
XM_011537877.3:c.6079A>T
|
XP_011536179.1:p.Met2027Leu
|
|
XM_017018787.1:c.2995A>T
|
XP_016874276.1:p.Met999Leu
|
|
XM_017018788.2:c.2341A>T
|
XP_016874277.1:p.Met781Leu
|
|
XM_024448833.1:c.4876A>T
|
XP_024304601.1:p.Met1626Leu
|
|
NM_198578.4:c.6079A>T
MANE Select
|
NP_940980.4:p.Met2027Leu
|
|