ENST00000264381.8:c.1793G>C
MANE Select
|
ENSP00000264381.3:p.Ser598Thr
|
|
ENST00000264381.7:c.1793G>C
|
ENSP00000264381.3:p.Ser598Thr
|
|
ENST00000479451.5:c.383G>C
|
ENSP00000418325.1:p.Ser128Thr
|
|
ENST00000482958.1:c.*299G>C
|
ENSP00000419804.1:n.*299G>C
|
|
ENST00000497011.5:c.*183G>C
|
ENSP00000419505.1:n.*183G>C
|
|
NM_000055.2:c.1793G>C
|
NP_000046.1:p.Ser598Thr
|
|
XM_005247685.1:c.1916G>C
|
XP_005247742.1:p.Ser639Thr
|
|
NM_000055.3:c.1793G>C
|
NP_000046.1:p.Ser598Thr
|
|
NR_137635.1:n.435G>C
|
|
|
NR_137636.1:n.2039G>C
|
|
|
NM_000055.4:c.1793G>C
MANE Select
|
NP_000046.1:p.Ser598Thr
|
|
NR_137635.2:n.386G>C
|
|
|
NR_137636.2:n.1990G>C
|
|
|