ENST00000706989.1:c.2509A>T
|
ENSP00000516702.1:p.Ser837Cys
|
|
ENST00000359125.7:c.2455A>T
MANE Select
|
ENSP00000352035.2:p.Ser819Cys
|
|
ENST00000637193.1:c.1852A>T
|
ENSP00000490734.1:p.Ser618Cys
|
|
ENST00000344462.8:c.2362A>T
|
ENSP00000339611.4:p.Ser788Cys
|
|
ENST00000357249.6:c.2023A>T
|
ENSP00000349789.3:p.Ser675Cys
|
|
ENST00000359125.6:c.2455A>T
|
ENSP00000352035.2:p.Ser819Cys
|
|
ENST00000360480.7:c.2371A>T
|
ENSP00000353668.3:p.Ser791Cys
|
|
ENST00000370224.5:c.2241+238A>T
|
ENSP00000359244.2:n.2241+238A>T
|
|
ENST00000625514.2:c.2205+238A>T
|
ENSP00000486040.1:n.2205+238A>T
|
|
ENST00000626839.2:c.2401A>T
|
ENSP00000486706.1:p.Ser801Cys
|
|
ENST00000629241.2:c.2133+238A>T
|
ENSP00000487142.1:n.2133+238A>T
|
|
ENST00000629676.2:c.1680-5965A>T
|
ENSP00000486194.1:n.1680-5965A>T
|
|
NM_004518.4:c.2371A>T
|
NP_004509.2:p.Ser791Cys
|
|
NM_172106.1:c.2401A>T
|
NP_742104.1:p.Ser801Cys
|
|
NM_172107.2:c.2455A>T
|
NP_742105.1:p.Ser819Cys
|
|
NM_172108.3:c.2362A>T
|
NP_742106.1:p.Ser788Cys
|
|
XM_006723787.1:c.2497A>T
|
XP_006723850.1:p.Ser833Cys
|
|
XM_011528807.1:c.2563A>T
|
XP_011527109.1:p.Ser855Cys
|
|
XM_011528808.1:c.2560A>T
|
XP_011527110.1:p.Ser854Cys
|
|
XM_011528809.1:c.2533A>T
|
XP_011527111.1:p.Ser845Cys
|
|
XM_011528810.1:c.2509A>T
|
XP_011527112.1:p.Ser837Cys
|
|
XM_011528811.1:c.2479A>T
|
XP_011527113.1:p.Ser827Cys
|
|
XM_011528812.1:c.2452A>T
|
XP_011527114.1:p.Ser818Cys
|
|
XM_011528813.1:c.2437A>T
|
XP_011527115.1:p.Ser813Cys
|
|
XM_011528814.1:c.2044A>T
|
XP_011527116.1:p.Ser682Cys
|
|
NM_004518.5:c.2371A>T
|
NP_004509.2:p.Ser791Cys
|
|
NM_172106.2:c.2401A>T
|
NP_742104.1:p.Ser801Cys
|
|
NM_172107.3:c.2455A>T
|
NP_742105.1:p.Ser819Cys
|
|
NM_172108.4:c.2362A>T
|
NP_742106.1:p.Ser788Cys
|
|
XM_011528810.2:c.2509A>T
|
XP_011527112.1:p.Ser837Cys
|
|
XM_011528811.2:c.2479A>T
|
XP_011527113.1:p.Ser827Cys
|
|
XM_017027841.2:c.2506A>T
|
XP_016883330.1:p.Ser836Cys
|
|
XM_017027842.2:c.2443A>T
|
XP_016883331.1:p.Ser815Cys
|
|
XM_017027843.1:c.2440A>T
|
XP_016883332.1:p.Ser814Cys
|
|
XM_017027844.2:c.2398A>T
|
XP_016883333.1:p.Ser800Cys
|
|
XM_017027845.1:c.1471A>T
|
XP_016883334.1:p.Ser491Cys
|
|
NM_004518.6:c.2371A>T
|
NP_004509.2:p.Ser791Cys
|
|
NM_172106.3:c.2401A>T
|
NP_742104.1:p.Ser801Cys
|
|
NM_172107.4:c.2455A>T
MANE Select
|
NP_742105.1:p.Ser819Cys
|
|
NM_172108.5:c.2362A>T
|
NP_742106.1:p.Ser788Cys
|
|
NM_001382235.1:c.2509A>T
|
NP_001369164.1:p.Ser837Cys
|
|