ENST00000706989.1:c.2550C>A
|
ENSP00000516702.1:p.Pro850=
|
|
ENST00000359125.7:c.2496C>A
MANE Select
|
ENSP00000352035.2:p.Pro832=
|
|
ENST00000637193.1:c.1893C>A
|
ENSP00000490734.1:p.Pro631=
|
|
ENST00000344462.8:c.2403C>A
|
ENSP00000339611.4:p.Pro801=
|
|
ENST00000357249.6:c.2064C>A
|
ENSP00000349789.3:p.Pro688=
|
|
ENST00000359125.6:c.2496C>A
|
ENSP00000352035.2:p.Pro832=
|
|
ENST00000360480.7:c.2412C>A
|
ENSP00000353668.3:p.Pro804=
|
|
ENST00000370224.5:c.2241+279C>A
|
ENSP00000359244.2:n.2241+279C>A
|
|
ENST00000625514.2:c.2205+279C>A
|
ENSP00000486040.1:n.2205+279C>A
|
|
ENST00000626839.2:c.2442C>A
|
ENSP00000486706.1:p.Pro814=
|
|
ENST00000629241.2:c.2133+279C>A
|
ENSP00000487142.1:n.2133+279C>A
|
|
ENST00000629676.2:c.1680-5924C>A
|
ENSP00000486194.1:n.1680-5924C>A
|
|
NM_004518.4:c.2412C>A
|
NP_004509.2:p.Pro804=
|
|
NM_172106.1:c.2442C>A
|
NP_742104.1:p.Pro814=
|
|
NM_172107.2:c.2496C>A
|
NP_742105.1:p.Pro832=
|
|
NM_172108.3:c.2403C>A
|
NP_742106.1:p.Pro801=
|
|
XM_006723787.1:c.2538C>A
|
XP_006723850.1:p.Pro846=
|
|
XM_011528807.1:c.2604C>A
|
XP_011527109.1:p.Pro868=
|
|
XM_011528808.1:c.2601C>A
|
XP_011527110.1:p.Pro867=
|
|
XM_011528809.1:c.2574C>A
|
XP_011527111.1:p.Pro858=
|
|
XM_011528810.1:c.2550C>A
|
XP_011527112.1:p.Pro850=
|
|
XM_011528811.1:c.2520C>A
|
XP_011527113.1:p.Pro840=
|
|
XM_011528812.1:c.2493C>A
|
XP_011527114.1:p.Pro831=
|
|
XM_011528813.1:c.2478C>A
|
XP_011527115.1:p.Pro826=
|
|
XM_011528814.1:c.2085C>A
|
XP_011527116.1:p.Pro695=
|
|
NM_004518.5:c.2412C>A
|
NP_004509.2:p.Pro804=
|
|
NM_172106.2:c.2442C>A
|
NP_742104.1:p.Pro814=
|
|
NM_172107.3:c.2496C>A
|
NP_742105.1:p.Pro832=
|
|
NM_172108.4:c.2403C>A
|
NP_742106.1:p.Pro801=
|
|
XM_011528810.2:c.2550C>A
|
XP_011527112.1:p.Pro850=
|
|
XM_011528811.2:c.2520C>A
|
XP_011527113.1:p.Pro840=
|
|
XM_017027841.2:c.2547C>A
|
XP_016883330.1:p.Pro849=
|
|
XM_017027842.2:c.2484C>A
|
XP_016883331.1:p.Pro828=
|
|
XM_017027843.1:c.2481C>A
|
XP_016883332.1:p.Pro827=
|
|
XM_017027844.2:c.2439C>A
|
XP_016883333.1:p.Pro813=
|
|
XM_017027845.1:c.1512C>A
|
XP_016883334.1:p.Pro504=
|
|
NM_004518.6:c.2412C>A
|
NP_004509.2:p.Pro804=
|
|
NM_172106.3:c.2442C>A
|
NP_742104.1:p.Pro814=
|
|
NM_172107.4:c.2496C>A
MANE Select
|
NP_742105.1:p.Pro832=
|
|
NM_172108.5:c.2403C>A
|
NP_742106.1:p.Pro801=
|
|
NM_001382235.1:c.2550C>A
|
NP_001369164.1:p.Pro850=
|
|