ENST00000706989.1:c.2510G>T
|
ENSP00000516702.1:p.Ser837Ile
|
|
ENST00000359125.7:c.2456G>T
MANE Select
|
ENSP00000352035.2:p.Ser819Ile
|
|
ENST00000637193.1:c.1853G>T
|
ENSP00000490734.1:p.Ser618Ile
|
|
ENST00000344462.8:c.2363G>T
|
ENSP00000339611.4:p.Ser788Ile
|
|
ENST00000357249.6:c.2024G>T
|
ENSP00000349789.3:p.Ser675Ile
|
|
ENST00000359125.6:c.2456G>T
|
ENSP00000352035.2:p.Ser819Ile
|
|
ENST00000360480.7:c.2372G>T
|
ENSP00000353668.3:p.Ser791Ile
|
|
ENST00000370224.5:c.2241+239G>T
|
ENSP00000359244.2:n.2241+239G>T
|
|
ENST00000625514.2:c.2205+239G>T
|
ENSP00000486040.1:n.2205+239G>T
|
|
ENST00000626839.2:c.2402G>T
|
ENSP00000486706.1:p.Ser801Ile
|
|
ENST00000629241.2:c.2133+239G>T
|
ENSP00000487142.1:n.2133+239G>T
|
|
ENST00000629676.2:c.1680-5964G>T
|
ENSP00000486194.1:n.1680-5964G>T
|
|
NM_004518.4:c.2372G>T
|
NP_004509.2:p.Ser791Ile
|
|
NM_172106.1:c.2402G>T
|
NP_742104.1:p.Ser801Ile
|
|
NM_172107.2:c.2456G>T
|
NP_742105.1:p.Ser819Ile
|
|
NM_172108.3:c.2363G>T
|
NP_742106.1:p.Ser788Ile
|
|
XM_006723787.1:c.2498G>T
|
XP_006723850.1:p.Ser833Ile
|
|
XM_011528807.1:c.2564G>T
|
XP_011527109.1:p.Ser855Ile
|
|
XM_011528808.1:c.2561G>T
|
XP_011527110.1:p.Ser854Ile
|
|
XM_011528809.1:c.2534G>T
|
XP_011527111.1:p.Ser845Ile
|
|
XM_011528810.1:c.2510G>T
|
XP_011527112.1:p.Ser837Ile
|
|
XM_011528811.1:c.2480G>T
|
XP_011527113.1:p.Ser827Ile
|
|
XM_011528812.1:c.2453G>T
|
XP_011527114.1:p.Ser818Ile
|
|
XM_011528813.1:c.2438G>T
|
XP_011527115.1:p.Ser813Ile
|
|
XM_011528814.1:c.2045G>T
|
XP_011527116.1:p.Ser682Ile
|
|
NM_004518.5:c.2372G>T
|
NP_004509.2:p.Ser791Ile
|
|
NM_172106.2:c.2402G>T
|
NP_742104.1:p.Ser801Ile
|
|
NM_172107.3:c.2456G>T
|
NP_742105.1:p.Ser819Ile
|
|
NM_172108.4:c.2363G>T
|
NP_742106.1:p.Ser788Ile
|
|
XM_011528810.2:c.2510G>T
|
XP_011527112.1:p.Ser837Ile
|
|
XM_011528811.2:c.2480G>T
|
XP_011527113.1:p.Ser827Ile
|
|
XM_017027841.2:c.2507G>T
|
XP_016883330.1:p.Ser836Ile
|
|
XM_017027842.2:c.2444G>T
|
XP_016883331.1:p.Ser815Ile
|
|
XM_017027843.1:c.2441G>T
|
XP_016883332.1:p.Ser814Ile
|
|
XM_017027844.2:c.2399G>T
|
XP_016883333.1:p.Ser800Ile
|
|
XM_017027845.1:c.1472G>T
|
XP_016883334.1:p.Ser491Ile
|
|
NM_004518.6:c.2372G>T
|
NP_004509.2:p.Ser791Ile
|
|
NM_172106.3:c.2402G>T
|
NP_742104.1:p.Ser801Ile
|
|
NM_172107.4:c.2456G>T
MANE Select
|
NP_742105.1:p.Ser819Ile
|
|
NM_172108.5:c.2363G>T
|
NP_742106.1:p.Ser788Ile
|
|
NM_001382235.1:c.2510G>T
|
NP_001369164.1:p.Ser837Ile
|
|